N/A
N=148
Warmed, Humidified Carbon Dioxide Insufflation vs Standard Carbon Dioxide in Laparoscopic Cholecystectomy
Cholecystolithiasis
Bottom Line
View on ClinicalTrials.gov: NCT01667848 ↗Enrolled (actual)
148
Serious AEs
0.0%
Results posted
Apr 2014
Primary outcome: Primary: Pain (Rated With a Visual Analog Scale for Pain)
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Optitherm® device activated (Device); Optitherm® device inactivated (Device)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- Kepler University Hospital
- Primary completion
- Jul 2013
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Pain (Rated With a Visual Analog Scale for Pain) |
2.22; 1.92 | — |
| PRIMARY Pain (Rated With a Visual Analog Scale for Pain) |
2.22; 1.92 | — |
| SECONDARY Core Temperature |
36.85; 37.07 | — |
| SECONDARY Core Temperature |
36.85; 37.07 | — |
Summary
The purpose of this study is to determine the effect of warmed, humidified carbon dioxide Insufflation vs standard carbon dioxide in laparoscopic cholecystectomy.
Eligibility Criteria
Inclusion Criteria
- Clinical diagnosis of cholecystolithiasis
Exclusion Criteria
- Clinical diagnosis of cholecystolithiasis with cholecystitis
Data sourced from ClinicalTrials.gov (NCT01667848). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.