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NCT01553422 Clinical Trial

Relation Between Intrabdominal Pressure and Collapsibility Index of Inferior Vena Cava Before and After Fluid Therapy

Abdominal Compartment Syndrome Clinical Trial

Official title:
Assessment of Relation Between Intrabdominal Pressure and Collapsibility Index of Inferior Vena Cava by Emergency Ultrasonography Before and After Fluid Therapy

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01553422
Other study ID # 390331
Secondary ID
Status Completed
Phase Phase 4
First received March 7, 2012
Last updated December 3, 2012
Start date March 2012
Est. completion date November 2012

Study information
Verified date December 2012
Source Isfahan University of Medical Sciences
Contact n/a
Is FDA regulated No
Health authority Iran: Ministry of Health
Study type Interventional

Clinical Trial Summary

This study assess the relation between intra abdominal pressure and collapsibility index of inferior vena cava in emergency bedside ultrasonography before and after fluid therapy.

Recruitment information / eligibility
Status Completed
Enrollment 82
Est. completion date November 2012
Est. primary completion date October 2012
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Body Mass index less than 30

- Written agree of the patient to participate in the study

Exclusion Criteria:

- neurogenic bladder or any documented previous surgery on bladder, spastic or contractile bladder

- large abdominal hernia

- patients who received neuromuscular blocking agents

- Patients with abdominal respiration due to chest pain

Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Diagnostic

Related Conditions & MeSH terms

Intervention

Other:
• Fluid therapy (Saline Normal)
Saline Normal 1 Lit. during 30 minutes
• Fluid therapy (Saline Normal)
saline Normal 1 lit during 30 minutes

Locations
Country Name City State
Iran, Islamic Republic of Emergency department, Alzahra General Hospital Isfahan

Sponsors (1)
Lead Sponsor Collaborator
Isfahan University of Medical Sciences

Country where clinical trial is conducted

Iran, Islamic Republic of, 

Outcome
Type Measure Description Time frame Safety issue
Primary Emergency bedside Ultrasonography assessment of Inferior Vena cava collapsibility index before and after fluid therapy "up to 36 weeks" Yes
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