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Trial details imported from ClinicalTrials.gov
For full trial details, please see the original record at
https://clinicaltrials.gov/study/NCT03875534
Registration number
NCT03875534
Ethics application status
Date submitted
7/03/2019
Date registered
14/03/2019
Titles & IDs
Public title
A Multi-center, Longitudinal, Observational Study of Children With Achondroplasia
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Scientific title
ACHieve: A Multi-center, Longitudinal, Observational Study of Children With Achondroplasia
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Secondary ID [1]
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TCC-NHS-01
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Achondroplasia
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Condition category
Condition code
Human Genetics and Inherited Disorders
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Other human genetics and inherited disorders
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Musculoskeletal
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Other muscular and skeletal disorders
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Intervention/exposure
Study type
Observational
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Patient registry
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Target follow-up duration
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Target follow-up type
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Description of intervention(s) / exposure
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Comparator / control treatment
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Control group
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Outcomes
Primary outcome [1]
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Annualized height velocity (centimeters/year) in children with achondroplasia
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Assessment method [1]
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Subjects will undergo a series of height measurements (in centimeters) on Day 1 and then every 6 months over the study period with height velocity reported in cm/year
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Timepoint [1]
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Up to 5 years
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Secondary outcome [1]
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Collection of natural history of achondroplasia symptoms in children with achondroplasia
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Assessment method [1]
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To characterize achondroplasia symptoms in children with achondroplasia
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Timepoint [1]
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Up to 5 years
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Eligibility
Key inclusion criteria
1. Legally authorized representative is willing and able to provide written, signed informed consent (with a written assent from the child when appropriate per local requirements)
2. Willing and able to comply with study protocol per investigator judgement
3. Clinical diagnosis of achondroplasia (confirmed by the investigator)
4. Age between 0 to 8 years old at enrollment
5. Able to stand without assistance (if the child is 24 months or older)
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Minimum age
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Years
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Maximum age
8
Years
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
1. Have received chronic treatment (> 3 months) of human growth hormone (hGH) or other medicinal products intended to affect stature or body proportionality at any time
2. Have received any dose of medicinal products intended to affect stature or body proportionality within the previous 6 months of screening
3. Have received any investigational medicinal product or device intended to affect stature or body proportionality at any time
4. History or presence of injury or disease of the growth plate(s), other than ACH, that affects growth potential of long bones
5. History of any bone-related surgery that affects growth potential of long bones, such as orthopedic reconstructive surgery and osteotomy (foramen magnum decompression, and laminectomy with full recovery are allowed with minimum of 6 months of bone healing. Limb-lengthening with full recovery is allowed with a minimum of 12 months of bone healing.)
6. Have forms of skeletal dysplasias other than achondroplasia or medical conditions that result in short stature or abnormal bone growth [such as severe achondroplasia with developmental delay and acanthosis nigricans (SADDAN), hypochondroplasia, growth hormone deficiency, Turner syndrome, pseudoachondroplasia. uncontrolled hypothyroidism, uncontrolled diabetes mellitus, autoimmune disease requiring corticosteroid therapy, inflammatory bowel disease, and chronic renal insufficiency]
7. History or presence of malignant disease, other than basal cell epithelioma/carcinoma or completely resected squamous skin cancer with no recurrence for 12 months per medical records
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Study design
Purpose
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Duration
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Selection
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Timing
Prospective
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Statistical methods / analysis
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Recruitment
Recruitment status
Completed
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Data analysis
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Reason for early stopping/withdrawal
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Other reasons
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Date of first participant enrolment
Anticipated
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Actual
19/06/2019
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
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Actual
12/01/2024
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Sample size
Target
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Accrual to date
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Final
260
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Recruitment in Australia
Recruitment state(s)
VIC
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Recruitment hospital [1]
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Ascendis Pharma Investigational Site - Parkville
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Recruitment postcode(s) [1]
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3052 - Parkville
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Recruitment outside Australia
Country [1]
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United States of America
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State/province [1]
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Arkansas
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Country [2]
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United States of America
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State/province [2]
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California
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Country [3]
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United States of America
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State/province [3]
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Colorado
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United States of America
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State/province [4]
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Delaware
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Country [5]
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United States of America
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State/province [5]
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Minnesota
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United States of America
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State/province [6]
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Missouri
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Country [7]
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United States of America
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New York
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United States of America
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Texas
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Country [9]
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United States of America
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State/province [9]
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Washington
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Country [10]
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United States of America
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State/province [10]
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Wisconsin
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Country [11]
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Austria
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State/province [11]
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Linz
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Country [12]
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Canada
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State/province [12]
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Alberta
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Country [13]
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Canada
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State/province [13]
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Ontario
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Country [14]
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Canada
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State/province [14]
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Quebec
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Country [15]
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China
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State/province [15]
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Beijing
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Country [16]
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China
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State/province [16]
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Guangzhou
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Country [17]
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China
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State/province [17]
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Hangzhou
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Country [18]
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China
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State/province [18]
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Shanghai
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Country [19]
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China
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State/province [19]
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Shenzhen
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Country [20]
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China
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Wuhan
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Denmark
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Hovedstaden
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France
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Paris
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Germany
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Berlin
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Ireland
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Dublin
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Italy
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State/province [25]
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Milano
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Country [26]
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New Zealand
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State/province [26]
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Auckland
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Country [27]
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Portugal
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State/province [27]
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Coimbra
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Country [28]
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Spain
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State/province [28]
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Barcelona
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Country [29]
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Spain
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State/province [29]
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Esplugues De Llobregat
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Country [30]
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Spain
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State/province [30]
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Madrid
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Country [31]
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Spain
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State/province [31]
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Vitoria-Gasteiz
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Country [32]
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Switzerland
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State/province [32]
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Lausanne
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Country [33]
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United Kingdom
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State/province [33]
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Glasgow
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Country [34]
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United Kingdom
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State/province [34]
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London
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Funding & Sponsors
Primary sponsor type
Commercial sector/industry
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Name
Ascendis Pharma A/S
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Address
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Country
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Ethics approval
Ethics application status
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Summary
Brief summary
This is a long-term, multi-center, longitudinal, observational study in children with achondroplasia (ACH). The aim is to study height velocity and comorbidities in children with ACH. This is a natural history study and no study medication will be administered.
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Trial website
https://clinicaltrials.gov/study/NCT03875534
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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Address
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Country
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Phone
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Fax
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Email
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Contact person for public queries
Name
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Address
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Phone
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Fax
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Email
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Contact person for scientific queries
Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
No
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No/undecided IPD sharing reason/comment
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What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
No documents have been uploaded by study researchers.
Results not provided in
https://clinicaltrials.gov/study/NCT03875534