Respiratory Restriction in Prader-Willi Syndrome

Completed

• Conditions: Prader-Willi Syndrome

• Registration Number: NCT06851351
• Lead Sponsor: Istituto Auxologico Italiano

Brief Summary

The main aim of this study is therefore to evaluate the impact of Prader Willi Syndrome (PWS) on lung and thoracoabdominal volumes, respiratory muscle strength and awake ventilatory pattern, and to quantify and localize the PWS-induced respiratory restriction.

Detailed Description

The aim is to study lung function in obese PWS patients using both volitional (spirometry, nitrogen wash-out, and maximal pressure measurements (MIP and MEP)) and non-volitional (awake ventilatory pattern by opto-electron plethysmography) tests, both in sitting and supine positions.

Spirometry, nitrogen wash-out, and MIP and MEP measurements are comprehensive assessments, while optoelectronic plethysmography allows restriction location through accurate measurement of thoracoabdominal volumes.

The results of the study could provide useful information about the calculation of the volumes enclosed by the grid of markers (in particular, the volume of the rib cage, which reflects the action of the intercostal muscles, the volume of the abdomen, which reflects the action of the diaphragm in the inspiratory phase and of the abdominal muscles during exhalation and their sum, which represents the total variation of the thoraco-abdominal wall. All these finds could be useful for respiratory rehabilitation protocols for obese PWS patients.

Study Timeline

• Study Start: 2024-01-16
• Primary Completion: 2024-07-05
• Study Completion: 2024-07-05
• Status Verified: 2025-02
• Study First Submitted: 2025-02-24
• Study First Submitted QC: 2025-02-24
• Last Update Submitted: 2025-02-24
• Study First Posted: 2025-02-28
• Last Update Posted: 2025-02-28

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 30

Inclusion Criteria

• Age 20-50 years
• Prader Willi Syndrome
• Body Mass Index > 30 kg/m2

Exclusion Criteria

• Lack of signed consent form

Control subjects

Inclusion Criteria:

• Age 20-50 years
• Body Mass Index < 25 kg/m2

Exclusion Criteria:

• Lack of signed consent form

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Rib cage contribution to ventilation	At enrollment	Percentage rib cage contribution to ventilation as measured by optoelectronic plethysmography

Trial Locations

Locations (1)

Istituto Auxologico Italiano IRCCS, Site Piancavallo; 🇮🇹 Oggebbio, Verbania, Italy