Laparoscopic Surgery in Elderly Patients
- Conditions
- Uterine Prolapse
- Interventions
- Other: laparoscopic surgery
- Registration Number
- NCT03095716
- Lead Sponsor
- University Hospital, Clermont-Ferrand
- Brief Summary
The primary purpose is to evaluate the quality of post-operative recovery and post-operative pain in elderly patients (more than 75 years) who undergo laparoscopic surgery for uterine prolapse.
- Detailed Description
Previous randomized clinical trial (NCT01887028) showed that the combined use of a low intraperitoneal pressure and a warmed, humidified CO2 gas resulted in better clinical outcomes (better quality of post-operative recovery and less post-operative pain) in patients aged 45-75 years, who underwent laparoscopic surgery for uterine prolapse.
Quality of post-operative recovery is very important in elderly patients. Investigators hypothesize that the combined use of a low intraperitoneal pressure and a warmed, humidified CO2 gas may also result in better clinical outcomes.
In this observational clinical trial, quality of post-operative recovery by QoR-40, post-operative pain by Visual Analog Scale, intra or postoperative complications and intraoperative core temperature are evaluated in elderly patients (more than 75 years old) who undergo laparoscopic surgery for uterine prolapse. Investigators use a low intraperitoneal pressure (6 mmHg) and a warmed, humidified CO2 gas during laparoscopy.
These outcomes will be compared with those of previous randomized clinical trial.
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- Female
- Target Recruitment
- 20
- Age more than 75 years old
- Patients undergoing laparoscopic promontofixation with or without sub-total hysterectomy for uterine prolapse
- ASA class I or II
- BMI more than 30
- Height less than 150cm
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description elderly patients laparoscopic surgery Impact of intraperitoneal pressure and warmed, humidified CO2 gas on clinical outcomes after laparoscopic surgery for uterine prolapse in patients aged ˃75 years
- Primary Outcome Measures
Name Time Method Quality of post-operative recovery assessed by the Quality of Recovery-40 questionnaire at 48h post-operatively Post-operative pain assessed by visual analogue scale in the word until discharge at 24h post-operatively Post-operative pain assessed by visual analogue scale in the postanesthesia care unit at 24h post-operatively
- Secondary Outcome Measures
Name Time Method post operative complications at 24h post-operatively Intraoperative core temperature at 24h post-operatively
Trial Locations
- Locations (1)
CHU Clermont-ferrand
🇫🇷Clermont-Ferrand, France