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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01616602
Other study ID # DVAMC-10-098
Secondary ID
Status Completed
Phase N/A
First received June 8, 2012
Last updated June 11, 2012

Study information

Verified date December 2011
Source Dallas VA Medical Center
Contact n/a
Is FDA regulated No
Health authority United States: Federal Government
Study type Interventional

Clinical Trial Summary

For obese patients, a randomized trial aimed at determining whether colonoscopy performance and patient comfort is improved if a patient is in the prone position (lay on their abdomen) versus the traditional left-sided position.


Recruitment information / eligibility

Status Completed
Enrollment 100
Est. completion date
Est. primary completion date
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- BMI >30kg/m2

- Elective Colonoscopy

Exclusion Criteria:

- Patients with prior colonic resection, strictures, or known colonic or intra-abdominal malignancy.

- Patients who are scheduled to have monitored or general anesthesia for their procedure.

- Emergency colonoscopy

- Inadequate preparation of the colon as assessed during colonoscopy

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind


Related Conditions & MeSH terms


Intervention

Other:
Prone Position
Patients were asked to lay on their abdomen for their elective colonoscopy.
Standard Position
The traditional left-lateral decubitus position

Locations

Country Name City State
United States Dallas VA Medical Center Dallas Texas

Sponsors (1)

Lead Sponsor Collaborator
Dallas VA Medical Center

Country where clinical trial is conducted

United States, 

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