Please note that the copy function is not enabled for this field.
If you wish to
modify
existing outcomes, please copy and paste the current outcome text into the Update field.
LOGIN
CREATE ACCOUNT
LOGIN
CREATE ACCOUNT
MY TRIALS
REGISTER TRIAL
FAQs
HINTS AND TIPS
DEFINITIONS
Trial Review
The ANZCTR website will be unavailable from 1pm until 3pm (AEDT) on Wednesday the 30th of October for website maintenance. Please be sure to log out of the system in order to avoid any loss of data.
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been endorsed by the ANZCTR. Before participating in a study, talk to your health care provider and refer to this
information for consumers
Download to PDF
Trial registered on ANZCTR
Registration number
ACTRN12605000484640
Ethics application status
Approved
Date submitted
13/09/2005
Date registered
23/09/2005
Date last updated
23/09/2005
Type of registration
Retrospectively registered
Titles & IDs
Public title
Efficacy study of Faulding's sea cucumer extracts in osteoarthritis.
Query!
Scientific title
Randomised, double-blind, three armed, placebo controlled trial comparing the safety and efficacy of sea cucumber extract, sea cucumber extract with Boswellia extract and placebo in adults with osteoarthritis.
Query!
Universal Trial Number (UTN)
Query!
Trial acronym
Query!
Linked study record
Query!
Health condition
Health condition(s) or problem(s) studied:
Osteoarthritis
606
0
Query!
Condition category
Condition code
Musculoskeletal
678
678
0
0
Query!
Osteoarthritis
Query!
Intervention/exposure
Study type
Interventional
Query!
Description of intervention(s) / exposure
Cucumaria frondosa extract 1000mg or Cucumaria frondosa extract 1000mg plus 400mg Boswellia serrata extract over 11 weeks.
Query!
Intervention code [1]
543
0
None
Query!
Comparator / control treatment
Placebo
Query!
Control group
Placebo
Query!
Outcomes
Primary outcome [1]
820
0
Change in clinical symptoms of osteoarthritis as measured by the WOMAC osteoarthritis index after 11 weeks treatment
Query!
Assessment method [1]
820
0
Query!
Timepoint [1]
820
0
After 11 weeks treatment
Query!
Secondary outcome [1]
1630
0
1) Change in clinical symptoms of osteoarthritis as measured by the Comprehensive Osteoarthritis Test (COAT).
Query!
Assessment method [1]
1630
0
Query!
Timepoint [1]
1630
0
After 11 weeks treatment.
Query!
Secondary outcome [2]
1631
0
2) Changes in platelet aggregation, euglobulin clot lysis times, lipid profiles and YKL-40.
Query!
Assessment method [2]
1631
0
Query!
Timepoint [2]
1631
0
After 11 weeks treatment.
Query!
Eligibility
Key inclusion criteria
1) Diagnosis of OA of the hip or knee. 2) Willing to discontinue all current OA treatment for the study duration commencing 4 weeks prior to baseline.
Query!
Minimum age
18
Years
Query!
Query!
Maximum age
85
Years
Query!
Query!
Sex
Both males and females
Query!
Can healthy volunteers participate?
No
Query!
Key exclusion criteria
1) Severe false alignment of the knee or hip2) Surgery or arthroscopy of the knee or hip within 2 months of baseline3) Infectious or inflammatory rheumatic disease4) Reliance on the use of lipolytic, fibrinolytic, anti-coagulant or anti-inflammatory agents5) A history of trauma associated with the affected joints6) Any condition that in the opinion of the investigator might interfere with the evaluation of the study objective.
Query!
Study design
Purpose of the study
Treatment
Query!
Allocation to intervention
Randomised controlled trial
Query!
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Study medications were supplied in numbered containers by the sponsor
Query!
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Computer generated block randomisation scheme
Query!
Masking / blinding
Blinded (masking used)
Query!
Who is / are masked / blinded?
Query!
Query!
Query!
Query!
Intervention assignment
Parallel
Query!
Other design features
Query!
Phase
Phase 2 / Phase 3
Query!
Type of endpoint/s
Safety/efficacy
Query!
Statistical methods / analysis
Query!
Recruitment
Recruitment status
Completed
Query!
Date of first participant enrolment
Anticipated
5/06/2000
Query!
Actual
Query!
Date of last participant enrolment
Anticipated
Query!
Actual
Query!
Date of last data collection
Anticipated
Query!
Actual
Query!
Sample size
Target
129
Query!
Accrual to date
Query!
Final
Query!
Recruitment in Australia
Recruitment state(s)
Query!
Funding & Sponsors
Funding source category [1]
750
0
Commercial sector/Industry
Query!
Name [1]
750
0
Faulding Healthcare Pty Ltd
Query!
Address [1]
750
0
Query!
Country [1]
750
0
Query!
Primary sponsor type
Commercial sector/Industry
Query!
Name
Faulding Healthcare Pty Ltd
Query!
Address
Query!
Country
Australia
Query!
Secondary sponsor category [1]
621
0
None
Query!
Name [1]
621
0
NA
Query!
Address [1]
621
0
Query!
Country [1]
621
0
Query!
Ethics approval
Ethics application status
Approved
Query!
Summary
Brief summary
Query!
Trial website
Query!
Trial related presentations / publications
Query!
Public notes
Query!
Contacts
Principal investigator
Name
36242
0
Query!
Address
36242
0
Query!
Country
36242
0
Query!
Phone
36242
0
Query!
Fax
36242
0
Query!
Email
36242
0
Query!
Contact person for public queries
Name
9732
0
Dr Phillip Cheras
Query!
Address
9732
0
Mater Health Services
Level 2
Community Services Building
South Brisbane QLD 4101
Query!
Country
9732
0
Australia
Query!
Phone
9732
0
+61 7 38406120
Query!
Fax
9732
0
+61 7 38406119
Query!
Email
9732
0
[email protected]
Query!
Contact person for scientific queries
Name
660
0
Dr Phillip Cheras
Query!
Address
660
0
Mater Health Services
Level 2
Community Services Building
South Brisbane QLD 4101
Query!
Country
660
0
Australia
Query!
Phone
660
0
+61 7 38406120
Query!
Fax
660
0
+61 7 38406119
Query!
Email
660
0
[email protected]
Query!
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
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
No additional documents have been identified.
Download to PDF