Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04700644
Other study ID # CAIPWS
Secondary ID
Status Completed
Phase
First received
Last updated
Start date May 15, 2020
Est. completion date June 6, 2020

Study information

Verified date January 2021
Source Medical University of Warsaw
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Introduction: The prevalence and clinical significance of central adrenal insufficiency (CAI) in adult patients with Prader Willi Syndrome (PWS) remains unclear. Aim: To assess the prevalence of CAI in adults with PWS and to analyse the effects of replacement therapy with hydrocortisone (HCT) in patients with suspected CAI. Material and Methods: Twenty one adult patients with PWS were evaluated. Based on peak cortisol at the 30 minute of the high dose short Synacthen test (HDSST), patients were divided into three groups: CAI (central adrenal insufficiency) - peak cortisol <500nmol/L, intermediate (partial AI) - peak cortisol ≥500 nmol/L and <600 nmol/L and AS (adrenal sufficiency) - peak cortisol ≥ 600 nmol/L. In patients with diagnosed CAI HCT replacement treatment was initiated. Body weight, body fat percentage, signs, and symptoms of CAI were evaluated after 6 and 12 months of treatment.


Recruitment information / eligibility

Status Completed
Enrollment 21
Est. completion date June 6, 2020
Est. primary completion date June 6, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years to 26 Years
Eligibility Inclusion Criteria: - PWS - age >=18 years Exclusion Criteria: - age <18 years - GC treatment at last 6 months

Study Design


Locations

Country Name City State
Poland Central Clinical Hospital Medical University of Warsaw Warsaw

Sponsors (1)

Lead Sponsor Collaborator
Medical University of Warsaw

Country where clinical trial is conducted

Poland, 

Outcome

Type Measure Description Time frame Safety issue
Primary The prevalence of CAI in adult PWS patients based on HDSST. The diagnosis of CAI was based on the high-dose short Synacthen test (HDSST). The following cut-off points were used:
CAI group (suspected CAI):
• cortisol < 500 nmol/L at the 30th minute
AS group (adrenal sufficiency - CAI excluded):
• cortisol = 600 nmol/L at the 30th minute
Intermediate group • cortisol =500 nmol/L and <600 nmol/L at the 30th minute
At first visit (before HCT treatment).
Primary Symptoms of CAI before hydrocortisone substitution: fatigue Incidence of the fatigue in the CAI, intermediate and the AS groups. Before HCT treatment
Primary Symptoms of CAI after 6 month hydrocorisone treatment: fatigue Incidence of the fatigue in the CAI, intermediate and the AS groups. After 6 month HCT treatment
Primary Symptoms of CAI after 12 month hydrocorisone treatment: fatigue Incidence of the fatigue in the CAI, intermediate and the AS groups. After 12 month HCT treatment
Primary Symptoms of CAI before hydrocortisone substitution: loss of appetite Incidence of loss of appetite in the CAI, intermediate and the AS groups. Before HCT treatment
Primary Symptoms of CAI after 6 month hydrocorisone treatment: loss of appetite Incidence of loss of appetite in the CAI, intermediate and the AS groups. After 6 month HCT treatment
Primary Symptoms of CAI after 12 month hydrocorisone treatment: loss of appetite Incidence of loss of appetite in the CAI, intermediate and the AS groups. After 12 month HCT treatment
Primary Symptoms of CAI before hydrocortisone substitution: muscle weakness Incidence of the muscle weakness in the CAI, intermediate and the AS groups. Before HCT treatment
Primary Symptoms of CAI after 6 month hydrocortisone treatment: muscle weakness Incidence of the muscle weakness in the CAI, intermediate and the AS groups. After 6 month HCT treatment
Primary Symptoms of CAI after 12 month hydrocortisone treatment: muscle weakness Incidence of the muscle weakness in the CAI, intermediate and the AS groups. After 12 month HCT treatment
Primary Symptoms of CAI before hydrocortisone substitution: myalgia Incidence of the myalgia in the CAI, intermediate and the AS groups. Before HCT treatment
Primary Symptoms of CAI after 6 month hydrocorisone treatment: myalgia Incidence of the myalgia in the CAI, intermediate and the AS groups. After 6 month HCT treatment
Primary Symptoms of CAI after 12 month hydrocorisone treatment: myalgia Incidence of the myalgia in the CAI, intermediate and the AS groups. After 12 month HCT treatment
Primary Symptoms of CAI before hydrocortisone substitution: arthralgia Incidence of the arthralgia in the CAI, intermediate and the AS groups. Before HCT treatment
Primary Symptoms of CAI after 6 month hydrocorisone treatment: arthralgia Incidence of the arthralgia in the CAI, intermediate and the AS groups. After 6 month HCT treatment
Primary Symptoms of CAI after 12 month hydrocorisone treatment: arthralgia Incidence of the arthralgia in the CAI, intermediate and the AS groups. After 12 month HCT treatment
Primary Symptoms of CAI before hydrocortisone substitution: weight loss Incidence of the weight loss (>3 kg) in the CAI, intermediate and the AS groups. Before HCT treatment
Primary Symptoms of CAI after 6 month hydrocorisone treatment: weight loss Incidence of the weight loss (>3 kg) in the CAI, intermediate and the AS groups. After 6 month HCT treatment
Primary Symptoms of CAI after 12 month hydrocorisone treatment: weight loss Incidence of the weight loss (>3 kg) in the CAI, intermediate and the AS groups. After 12 month HCT treatment
Primary Symptoms of CAI before hydrocortisone substitution: nausea Incidence of the nausea in the CAI, intermediate and the AS groups. Before HCT treatment
Primary Symptoms of CAI after 6 month hydrocorisone treatment: nausea Incidence of the nausea in the CAI, intermediate and the AS groups. After 6 month HCT treatment
Primary Symptoms of CAI after 12 month hydrocorisone treatment: nausea Incidence of the nausea in the CAI, intermediate and the AS groups. After 12 month HCT treatment
Primary Symptoms of CAI before hydrocortisone substitution: vomiting Incidence of the vomiting in the CAI, intermediate and the AS groups. Before HCT treatment
Primary Symptoms of CAI after 6 month hydrocorisone treatment: vomiting Incidence of the vomiting in the CAI, intermediate and the AS groups. After 6 month HCT treatment
Primary Symptoms of CAI after 12 month hydrocorisone treatment: vomiting Incidence of the vomiting in the CAI, intermediate and the AS groups. After 12 month HCT treatment
Primary Symptoms of CAI before hydrocortisone substitution: abdominal pain Incidence of the abdominal pain in the CAI, intermediate and the AS groups. Before HCT treatment
Primary Symptoms of CAI after 6 month hydrocorisone treatment: abdominal pain Incidence of the abdominal pain in the CAI, intermediate and the AS groups. After 6 month HCT treatment
Primary Symptoms of CAI after 12 month hydrocorisone treatment: abdominal pain Incidence of the abdominal pain in the CAI, intermediate and the AS groups. After 12 month HCT treatment
Primary BMI before hydrocortisone substitution in PWS patients with CAI Measurement of weight and height will be combined to report BMI in kg/m^2. Before HCT treatment
Primary BMI after 6 month hydrocortisone substitution in PWS patients with CAI Measurement of weight and height will be combined to report BMI in kg/m^2. After 6 month HCT treatment
Primary BMI after 12 month hydrocortisone substitution in PWS patients with CAI Measurement of weight and height will be combined to report BMI in kg/m^2. After 12 month HCT treatment
Primary Body fat percentage before hydrocortisone substitution in PWS patients with CAI Measurement of the body fat percentage using bioelectrical impedance method. Before HCT treatment
Primary Body fat percentage after 6 month hydrocortisone substitution in PWS patients with CAI Measurement of the body fat percentage using bioelectrical impedance method. After 6 month HCT treatment
Primary Body fat percentage after 12 month hydrocortisone substitution in PWS patients with CAI Measurement of the body fat percentage using bioelectrical impedance method. After 12 month HCT treatment
Secondary Concentration of morning cortisol Results of morning cortisol in the entire study group. At first visit (before HCT treatment).
Secondary Concentration of ACTH Results of ACTH in the entire study group. At first visit (before HCT treatment).
Secondary Concentration of dihydroepiandrosterone sulfate Results of dihydroepiandrosterone sulfate measurements in the entire study group. At first visit (before HCT treatment).
Secondary Laboratory findings - short Synacthen test Results of the short Synacthen test in the entire study group. At first visit (before HCT treatment).
See also
  Status Clinical Trial Phase
Recruiting NCT05032326 - Long-term Interventional Follow-up Study of Children With Prader-Willi Syndrome Included in the OTBB3 Clinical Trial Phase 3
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