Skip to content

Comparative Ultrasonic Study of Post Operative Diaphragmatic Dysfunction in Abdominal and Head and Neck Surgery

Comparative Ultrasonic Study of Post Operative Diaphragmatic Dysfunction in Abdominal and Head and Neck Surgery

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01737775
Acronym
Under the Dome
Enrollment
43
Registered
2012-11-30
Start date
2012-10-31
Completion date
2013-08-31
Last updated
2013-08-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diaphragmatic Dysfunction

Keywords

diaphragmatic dysfunction, ultrasonography, respiratory distress, abdominal surgery, Age, gender, biometric, body mass index, ASA score, smoking status, history of respiratory disease

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).

Interventions

PROCEDUREDiaphragmatic amplitude measurement

Diaphragmatic amplitude is measured by M Mode ultrasonography the day before and after surgery

Sponsors

Hospices Civils de Lyon
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frame
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

MeasureTime frame
All cause morbiditywithin the first 28 days after surgery

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026