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Trial details imported from ClinicalTrials.gov
For full trial details, please see the original record at
https://clinicaltrials.gov/study/NCT04484051
Registration number
NCT04484051
Ethics application status
Date submitted
15/07/2020
Date registered
23/07/2020
Date last updated
16/02/2023
Titles & IDs
Public title
Growth Hormone Study in Adults With Prader-Willi Syndrome
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Scientific title
Growth Hormone Study in Adults With Prader-Willi Syndroom
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Secondary ID [1]
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GAP
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Universal Trial Number (UTN)
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Trial acronym
GAP
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Peripheral Neuropathic Pain
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0
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Condition category
Condition code
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
Eligibility
Key inclusion criteria
* The patient is diagnosed with Prader-Willi syndrome (genetically confirmed)
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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
* Non cooperative behaviour
* Pregnancy
* Known malignancies
* Poorly controlled diabetes (HbA1c > 64 mmol/mol (8%))
* Untreated obstructive sleep apnea (apnea-hypopnea index > 5)
* Body mass index above 40 kg/m2
* Upper-airway obstruction of any cause
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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
Not yet recruiting
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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
24/03/2023
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Actual
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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
1/10/2026
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Actual
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Sample size
Target
25
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
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Funding & Sponsors
Primary sponsor type
Other
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Name
Erasmus Medical Center
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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
The overall objective of this study is to measure the effect of growth hormone (GH) treatment on physical and psychosocial health in adults with Prader-Willi syndrome. Adults with PWS who have not been treated with GH during the past three years and who will start with GH treatment as part of regular patient care will be asked for informed consent to participate in this open-label prospective cohort study. We hypothesize that growth hormone treatment will improve the physical and psychosocial health.
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Trial website
https://clinicaltrials.gov/study/NCT04484051
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Trial related presentations / publications
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Public notes
This record is viewable in the ANZCTR as it had previously listed Australia and/or New Zealand as a recruitment site, however these sites have since been removed
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Contacts
Principal investigator
Name
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Laura de Graaff, MD, PhD
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Address
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Erasmus MC, University Medical Center Rotterdam
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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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Laura de Graaff, MD, PhD
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Address
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Country
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Phone
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0031618843010
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Fax
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Email
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[email protected]
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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/NCT04484051
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