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Clinical Trial Summary

To assess the safety and efficacy of CO2 insufflations during ERCP

1. Primary objective:

To assess the patient's symptoms, abdominal pain and abdominal distension post procedure (ERCP) in the study group.

2. Secondary objective:

Endoscopist:

- To assess the adequacy of bowel distension for adequate luminal visualization

- To assess the peristaltic movement during the ERCP

Anesthetist:

- To measure the PCO2 level in patient post procedure.

- To assess the amount of sedation required during the procedure.

- To assess saturation and vital signs through out the procedure.

- To assess requirement of buscopan.


Clinical Trial Description

mentioned in complete ;


Study Design

Observational Model: Case Control, Time Perspective: Prospective


Related Conditions & MeSH terms


NCT number NCT01321203
Study type Observational
Source Asian Institute of Gastroenterology, India
Contact
Status Completed
Phase N/A
Start date August 2010
Completion date March 2011

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