Comparative Ultrasonic Study of Post Operative Diaphragmatic Dysfunction in Abdominal and Head and Neck Surgery
Not Applicable
Completed
- Conditions
- Diaphragmatic Dysfunction
- Interventions
- Procedure: Diaphragmatic amplitude measurement
- Registration Number
- NCT01737775
- Lead Sponsor
- Hospices Civils de Lyon
- Brief Summary
Diaphragmatic dysfunction (DD) is one of the main risk factors for post operative respiratory distress syndrome. Ultrasonography is a diagnosis tool for DD but few studies have been published. The aim of this prospective study is to compare the achievement of diaphragmatic function depending on the type of surgery (abdominal and head and neck surgery).
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 43
Inclusion Criteria
- Age>18 years
- Upper abdominal or head and neck surgery
- written consent
Exclusion Criteria
- Age <18 years
- Pregnancy
- History of neuropathy or myopathy,
- History of diaphragm paralysis, thoracic surgery, pneumothorax, pneumomediastinum
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Abdominal laparoscopic surgery (C group) Diaphragmatic amplitude measurement - Abdominal surgery by laparotomy (L group) Diaphragmatic amplitude measurement - Head and neck surgery (O group) Diaphragmatic amplitude measurement -
- Primary Outcome Measures
Name Time Method Comparison of diaphragmatic amplitude measured by M-Mode ultrasonography performed the day before and the day after surgery in 3 groups: laparoscopic abdominal surgery, abdominal surgery by laparotomy and head and neck surgery. two months
- Secondary Outcome Measures
Name Time Method All cause morbidity within the first 28 days after surgery
Trial Locations
- Locations (1)
Département d'Anesthésie Hôpital de la Croix Rousse
🇫🇷Lyon, France