NCT01667848View on ClinicalTrials.gov

Warmed, Humidified Carbon Dioxide Insufflation vs Standard Carbon Dioxide in Laparoscopic Cholecystectomy

NACompletedINTERVENTIONAL
Enrollment

148

Participants

Timeline

Start Date

July 31, 2011

Primary Completion Date

July 31, 2013

Study Completion Date

September 30, 2013

Conditions
Cholecystolithiasis
Interventions
DEVICE

Optitherm® device activated

The use of Optitherm® device, which was attached to the insufflation equipment in all of the patients but was only activated by the single scrub nurse in those patients randomized to group B.

DEVICE

Optitherm® device inactivated

The use of Optitherm® device, which was attached to the insufflation equipment in all of the patients but was inactivated in group A.

Trial Locations (1)

4020

2nd Surgical Department, Academic Teaching Hospital, AKH Linz, Linz

All Listed Sponsors
lead

Kepler University Hospital

OTHER

NCT01667848 - Warmed, Humidified Carbon Dioxide Insufflation vs Standard Carbon Dioxide in Laparoscopic Cholecystectomy | Biotech Hunter | Biotech Hunter