POPS3: Frequency of Pompe's Disease and Neuromuscular Etiologies in Patients With Restrictive Respiratory Failure Associated With Signs of Muscle Weakness

Sponsor
Centre Hospitalier Universitaire de Nice (Other)
Overall Status
Unknown status
CT.gov ID
NCT02746718
Collaborator
(none)
500
21
1
48
23.8
0.5

Study Details

Study Description

Brief Summary

A breach of respiratory function may be one of the elements more or less early or predominant clinical picture of neuromuscular diseases. It is considered that the obstructive syndromes represent 64% and restrictive or mixed syndromes 36% of chronic respiratory insufficiency, approximately 7% due to a neuromuscular disease. The frequency and type of impairment are dependent on the underlying pathology.

The neuromuscular restrictive respiratory failure (IRR) remains partially unknown pulmonologists, especially because the signs of muscle weakness are sometimes difficult to detect. However, respiratory diseases are a major concern in neuromuscular diseases because they can have an impact both on sleep (not sleep, ...) on the daily activities (breathlessness on exertion, dyspnea) and thereby alter the quality of life of patients. Moreover, they represent a significant morbidity and mortality factor. Chest tightness may in some cases reveal the disease and thus constitute the chief complaint of a patient with a neuromuscular disease. In late-onset Pompe disease, lung disease is the predominant clinical symptoms in about 30% of patients.

An algorithm was developed to guide practitioners and help them in their diagnostic approach to the cause of the IRR (diagnostic algorithm ATS / ERS 2005). However, this algorithm does not allow precise identification of the neuromuscular causes.

At the patient level, this can have an impact by extending the time before placing a diagnosis. In Pompe disease, the average time to diagnosis reached 7.9 years. However, there are for this disease a simple and rapid diagnostic test. Therefore, a greater awareness of practitioners with regard to the particular Pompe disease and neuromuscular diseases in general may be beneficial to patients.

This study aims to:
  1. awareness pulmonologists to the possibility of neuromuscular an IRR.

  2. characterize the frequency of neuromuscular origin of IRR in a broad population of patients with concomitant signs muscle weakness.

  3. reduce the time to diagnosis by directing patients to neuromuscular reference center early.

Condition or Disease Intervention/Treatment Phase
  • Other: Blood sample
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
500 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Diagnostic
Official Title:
Frequency of Pompe's Disease and Neuromuscular Etiologies in Patients With Restrictive Respiratory Failure Associated With Signs of Muscle Weakness
Actual Study Start Date :
Dec 11, 2015
Anticipated Primary Completion Date :
Dec 11, 2019
Anticipated Study Completion Date :
Dec 11, 2019

Arms and Interventions

Arm Intervention/Treatment
Other: Restrictive Respiratory Failure

A CPK dosage, muscular questionnaires and a Pompe Disease test are practiced on patient with Restrictive Respiratory Failure without etiology

Other: Blood sample
A blood sample for CPK dosage and pompe disease test

Outcome Measures

Primary Outcome Measures

  1. Number of new cases of Pompe disease diagnosed by a positive DBS [At the inclusion]

    Number of new cases of Pompe disease diagnosed by a positive DBS in patients with unexplained restriction pulmonaires.ries volumes, the patient is adressed to a specialist to dertermine etilogy of the muscular disease.

Secondary Outcome Measures

  1. Number of new cases and etiologies of neuromuscular diseases diagnosed in patients with unexplained restriction of lung volumes [at 6 month]

    If a patient have an high CPK rate or a blotter test positive for Pompe disease or a suspicion of muscular disease with the muscular questionnaires, the patient is addressed to a specialist to determine etiology of the muscular disease.

  2. Frequency and description of neurological symptoms associated with neuromuscular diseases to respiratory revelation [at 6 month]

    If a patient have an high CPK rate or a suspicion of muscular disease with the muscular questionnaires, the patient is addressed to a specialist to determine etiology of the muscular disease.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Presence of a CV <80% of predicted and / or <LIN

  • Presence spirometry a report Tiffeneau (FEV / CV) equal to or higher than normal

  • Signature of informed consent

  • Men and women age ≥ 18 years

  • Production of a medical examination

  • Affiliated to social security

Exclusion Criteria:
  • restrictive breath traumatic

  • restrictive respiratory failure associated with parenchymal disorder, whether localized or diffuse

  • known neuromuscular disease associated with a restrictive lung disease

  • Patient under guardianship, curatorship, protected by law

  • Inability to cooperate

  • Morbid obesity with a BMI ≥40

Contacts and Locations

Locations

Site City State Country Postal Code
1 CHU d'Angers Angers France
2 Centre hospitalier d'Argenteuil Argenteuil France
3 CHU de Brest Brest France 29609
4 CH d'Escartons Briancon France
5 CH de Cannes Cannes France
6 CHI de Créteil Créteil France 94000
7 CHU le Bocage Dijon France
8 CHRU de Lille Lille France
9 CHU de Limoges Limoges France
10 Cabinet Dr Pereira-Cortese Nice France
11 CHU de Nice Nice France
12 GH Pitié Salpêtrière Paris France
13 Hôpital Raymond Poincaré Paris France
14 Hôpital Saint Louis Paris France
15 Hôpital Tenon Paris France
16 Polyclinique les Bleuets Reims France
17 CHU de Rouen Rouen France
18 CHU de St Etienne Saint-Étienne France 94000
19 CHU de Toulouse Toulouse France
20 CHRU de Tours Tours France 37044
21 Clinique Saint Joseph Trélazé France 49800

Sponsors and Collaborators

  • Centre Hospitalier Universitaire de Nice

Investigators

  • Principal Investigator: Sabrina Sacconi, Centre Hospitalier Universitaire de Nice

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Centre Hospitalier Universitaire de Nice
ClinicalTrials.gov Identifier:
NCT02746718
Other Study ID Numbers:
  • 14-PP-13
First Posted:
Apr 21, 2016
Last Update Posted:
Mar 19, 2018
Last Verified:
Mar 1, 2018
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 19, 2018