Prader-Willi Syndrome Clinical Trial
— OTBB3-FUOfficial title:
Long-term Interventional Follow-up Study up to 4 Years of Age of Children With Prader-Willi Syndrome Included in the OTBB3 Clinical Trial and Comparison With an Untreated Cohort of Children With Prader-Willi Syndrome
This study is a prospective, multicentre, interventional cohort study in children with Prader-Willi Syndrome (PWS) over 4 years (no treatment administered). The duration of the preceding OTTB3 study is 26 weeks. An untreated cohort of children with PWS will be included at an age of 2 years and followed up until an age of 4 years. Regarding the untreated cohort, children with PWS born in France and too old to be recruited in OTBB3 trial, principally those who were born within one year before the start of OTBB3 trial, will be offered to participate in this study. Infants born later who couldn't be included in OTBB3 study will be also offered to participate.
Status | Recruiting |
Enrollment | 80 |
Est. completion date | April 1, 2025 |
Est. primary completion date | April 1, 2025 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 12 Months to 36 Months |
Eligibility | Inclusion Criteria: 1. Male or female child with a genetically confirmed diagnosis of PWS (patients can be enrolled if the genetic subtype is not available at inclusion, but the genetic subtype needs to be confirmed during the study); 2. The parents (or legal representative) must have signed the consent form; 3. Treated cohort: the child participated in the OTBB3 study and is aged 16±4 months at inclusion, 4. Untreated cohort: the child has never received OT, is aged 30±6 months at inclusion (in order to maximise the number of children in the untreated cohort) and is followed in France. Exclusion Criteria: 1. Administrative problems: 1. Inability for the parents (or legal representative) to understand/fulfil study requirements; 2. No coverage by a social security regime; 2. Refusal of parents (or legal representative) to sign the consent form; |
Country | Name | City | State |
---|---|---|---|
France | Hôpital Femme Mère Enfant | Bron | |
France | CHU Dijon Hôpital des Enfants | Dijon | |
France | CHU de Grenoble | Grenoble | |
France | Hôpital Jeanne de Flandre | Lille | |
France | Hôpital de la Timone Enfant | Marseille | |
France | CHU Nancy | Nancy | |
France | CHU Nantes | Nantes | |
France | Hôpital CHU-Lenval | Nice | |
France | Groupe Hospitalier Necker - Enfants Malades | Paris | |
France | CHU Rennes | Rennes | |
France | CHU Rouen | Rouen | |
France | Centre de réfrence Prader-Willi, Hospital of infants | Toulouse |
Lead Sponsor | Collaborator |
---|---|
University Hospital, Toulouse |
France,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Confirmation of the long term safety profile (1) | The number of patients with adverse events (AEs) | 4 years | |
Primary | Confirmation of the long term safety profile (2) | The percentage of patients with adverse events (AEs) | 4 years | |
Primary | Confirmation of the long term safety profile (3) | Assessment in the treated cohort of the occurrence of the main comorbidities in Prader Willi Syndrome | 4 years | |
Primary | Confirmation of the long term safety profile (4) | Assessment in the treated cohort of:
The occurrence of medications, surgery and rehabilitations by collecting type, age (years) at start and stop, dosing or frequency |
4 years | |
Secondary | Complete the safety assessment by the description of the development of the child (1.1) | Assessment in the treated cohort of: weight (kilograms) | 4 years | |
Secondary | Complete the safety assessment by the description of the development of the child (1.2) | Assessment in the treated cohort of: height (meters) | 4 years | |
Secondary | Complete the safety assessment by the description of the development of the child (1.3) | Assessment in the treated cohort of: BMI (kg/m^2) | 4 years | |
Secondary | Complete the safety assessment by the description of the development of the child (2.1) | Assessment in the treated cohort of Child development: age at which sitting has been reached | 4 years | |
Secondary | Complete the safety assessment by the description of the development of the child (2.2) | Assessment in the treated cohort of Child development: age at which crawling has been reached | 4 years | |
Secondary | Complete the safety assessment by the description of the development of the child (2.3) | Assessment in the treated cohort of Child development: age at which walking has been reached | 4 years | |
Secondary | Complete the safety assessment by the description of the development of the child (2.4) | Assessment in the treated cohort of Child development: age at which running has been reached | 4 years | |
Secondary | Complete the safety assessment by the description of the severity of the disease | Severity of the disease for:
Eating disorders by using Hyperphagia Questionnaire for Clinical Trials (HQCT); |
4 years | |
Secondary | Complete the safety assessment by the description of the severity of the disease (2) | Severity of the disease for:
Psychiatric disorders by using the Child Behaviour Checklist (CBCL); |
4 years | |
Secondary | Assessment of endocrine disorders by IGF1 | Analysis of plasma Insulin-like growth factor 1 (IGF1, ng/mL) | 4 years | |
Secondary | Assessment of endocrine disorders by TSH | Analysis of plasma thyroid stimulating hormone (TSH, µUI/mL) | 4 years |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT04526379 -
Study of Emotion and Cognition Abilities of Children With PWS and Proposition of an Innovative Remediation
|
N/A | |
Terminated |
NCT03458416 -
A Study to Assess the Long-Term Safety of Pharmaceutical Grade Synthetic Cannabidiol Oral Solution in Participants With Prader-Willi Syndrome
|
Phase 2 | |
Completed |
NCT03718416 -
Natural History Study of Serious Medical Events in PWS
|
||
Completed |
NCT05322096 -
Study to Evaluate Efficacy, Safety, and Tolerability of RGH-706 in Prader-Willi Syndrome
|
Phase 2 | |
Completed |
NCT02205450 -
Growth Hormone in Children Under 2 Years With Prader-Willi in Hospital of Sabadell
|
||
Terminated |
NCT02179151 -
Double-Blind, Placebo Controlled, Phase 3 Trial of ZGN-440 (Beloranib) in Obese Subjects With Prader-Willi Syndrome
|
Phase 3 | |
Completed |
NCT00375089 -
Characteristics of Prader-Willi Syndrome and Early-onset Morbid Obesity
|
N/A | |
Completed |
NCT00004351 -
Study of Phenotype and Genotype Correlations in Patients With Contiguous Gene Deletion Syndromes
|
N/A | |
Recruiting |
NCT05938543 -
Cerebellar TMS and Satiety in Prader-Willi Syndrome
|
N/A | |
Suspended |
NCT05879614 -
An Open-Label Study of Oral NNZ-2591 in Prader-Willi Syndrome (PWS-001)
|
Phase 2 | |
Recruiting |
NCT03031626 -
Oxygen Versus Medical Air for Treatment of CSA in Prader Will Syndrome
|
Phase 4 | |
Withdrawn |
NCT04086810 -
An Open-Label Study of DCCR Tablet in Patients With PWS
|
Phase 3 | |
Completed |
NCT02629991 -
Oxytocin vs. Placebo for the Treatment Hyperphagia in Children and Adolescents With Prader-Willi Syndrome
|
Phase 2 | |
Recruiting |
NCT02297022 -
Deep Brain Stimulation for the Treatment of Obesity in Patients With Prader-Willi Syndrome
|
Phase 1 | |
Not yet recruiting |
NCT02263781 -
PREPL in Health and Disease
|
N/A | |
Completed |
NCT00551343 -
Gut Derived Hormones, Body Composition and Metabolism in Prader-Willi Syndrome
|
N/A | |
Recruiting |
NCT06448871 -
Ultrasound to Assess Sarcopenia in Prader Willi Syndrome
|
||
Enrolling by invitation |
NCT03655223 -
Early Check: Expanded Screening in Newborns
|
||
Recruiting |
NCT05939453 -
Impact of Bright Light Therapy on Prader-Willi Syndrome
|
N/A | |
Recruiting |
NCT04463316 -
GROWing Up With Rare GENEtic Syndromes
|