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Trial details imported from ClinicalTrials.gov
For full trial details, please see the original record at
https://clinicaltrials.gov/study/NCT00622583
Registration number
NCT00622583
Ethics application status
Date submitted
14/02/2008
Date registered
25/02/2008
Date last updated
5/06/2023
Titles & IDs
Public title
International Hernia Mesh Registry
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Scientific title
A Two-Year Follow-up, Post-Implantation, Multi-center, International Hernia Mesh Registry
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Secondary ID [1]
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200-06-007
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Universal Trial Number (UTN)
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Trial acronym
IHMR
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Hernia
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Condition category
Condition code
Oral and Gastrointestinal
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Other diseases of the mouth, teeth, oesophagus, digestive system including liver and colon
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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
Observation Group - Subjects who meet the inclusion/exclusion criteria who have had a hernia repair.
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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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Recurrence of the hernia
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Assessment method [1]
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Timepoint [1]
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1 month, 6-months, 12 months, 2 years
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Primary outcome [2]
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Pain assessment scores by patients for the duration of the registry (Acute pain and Chronic pain)
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Assessment method [2]
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Timepoint [2]
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1 month, 6-months, 12 months, 2 years
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Secondary outcome [1]
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Assessment of post-operative complications/safety
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Assessment method [1]
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Timepoint [1]
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At the time of surgery
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Secondary outcome [2]
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Assessment of procedure time
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Assessment method [2]
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Timepoint [2]
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At the time of surgery
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Eligibility
Key inclusion criteria
Inclusion Criteria
Patients must satisfy the following criteria before entering the registry:
1. Provide written informed consent prior to surgery;
2. Male or female patients that are > 18 years of age;
3. Be literate and able to understand a language available in the Registry Patient Questionnaires;
4. Scheduled to receive a surgically implanted ETHICON synthetic mesh using any fixation method or a non-ETHICON synthetic mesh which must be fixated with SECURESTRAP® or SECURESTRAP® Open for repair of a hernia defect;
5. Agree to provide long-term, outcomes data to Quintiles Outcome;
6. Agree to provide contact information;
7. Two or more pieces of the same mesh product sewn together will be considered as one mesh, and is therefore allowed in this registry
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Minimum age
18
Years
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Maximum age
No limit
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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
Exclusion Criteria
Patients who meet any of the following criteria will be excluded from participating in the registry:
1. Patients that are <18 years of age;
2. Patients who have been entered into the registry previously;
3. Employees of the investigator or registry center with direct involvement in the proposed registry or other studies under the direction of that investigator or registry center and employees of ETHICON;
4. Patients suffering from and currently receiving medication for chronic pain (defined as suffering pain for greater than 3 months);
5. Patients known to be suffering from pre-existing chronic depression;
6. Patients currently known or suspected to abuse drugs or alcohol;
7. Patients suffering from a terminal illness (e.g. cancer);
8. Patients requiring multiple hernia repairs (including bilateral inguinal/femoral);
9. Patients requiring any other (concomitant) surgical procedure;
10. Patients suffering from an ongoing infection, sepsis, contaminated mesh or fistulas;
11. Patients who require hiatal, paraesophageal or diaphragmatic hernia repair;
12. Patients requiring two different types of meshes;
13. Patients requiring two or more meshes not sewn together
14. Patients scheduled to receive a surgically implanted biologic mesh product for repair of a hernia defect
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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
1/09/2007
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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
25/01/2021
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Sample size
Target
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Accrual to date
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Final
5179
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Recruitment in Australia
Recruitment state(s)
SA,WA
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Recruitment hospital [1]
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Queen Elizabeth Hospital - Woodville
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Recruitment hospital [2]
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MercyCare Mount Lawley Hospital - Mount Lawley
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Recruitment hospital [3]
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The Wesley Hospital - Auchenflower
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Recruitment postcode(s) [1]
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5011 - Woodville
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Recruitment postcode(s) [2]
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6050 - Mount Lawley
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Recruitment postcode(s) [3]
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QLD 4066 - Auchenflower
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Recruitment outside Australia
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United States of America
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Florida
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Massachusetts
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Missouri
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New York
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North Carolina
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Oklahoma
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Oregon
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Texas
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Virginia
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Belgium
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Bonheiden
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Belgium
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Gent
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Canada
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Ontario
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China
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Shanghai
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France
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Antony Cedex
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France
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Avignon
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France
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Clermont-Ferrand
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France
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Lomme
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France
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Lyon
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France
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Marseille
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France
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Nancy
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France
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Nice
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France
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Paris
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France
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Reims
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Germany
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Neuss
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Italy
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Rome
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Hertogenbosch
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South Africa
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Cape Town
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Aviles
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Spain
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Sweden
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Sodertalje
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Cambrideshire
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Somerset
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Ayr
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Dorchester
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Farnworth
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London
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North Shields
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Northampton
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United Kingdom
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Paisley
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Funding & Sponsors
Primary sponsor type
Commercial sector/industry
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Name
Ethicon, Inc.
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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 an open-label, multi-center, long-term, prospective hernia mesh registry. A minimum of 4,800 hernia patients will be enrolled from approximately 60 active sites globally
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Trial website
https://clinicaltrials.gov/study/NCT00622583
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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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Niels-Derrek Schmitz, M.D.
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Address
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Ethicon, Inc.
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Fax
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Email
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Contact person for public queries
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Contact person for scientific queries
No information has been provided regarding IPD availability
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/NCT00622583
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