Vaginal Hysterectomy, Laparoscopic Hysterectomy, Postoperative Pain
Not Applicable
Completed
- Conditions
- Postoperative Pain
- Interventions
- Procedure: laparoscopy, laparoscopic hysterectomy
- Registration Number
- NCT01442961
- Lead Sponsor
- Tampere University Hospital
- Brief Summary
The previous studies have shown that recovery after laparoscopic or vaginal hysterectomy is faster than after abdominal approach. The aim of this study is to evaluate postoperative pain after vaginal or laparoscopic hysterectomy. The primary outcome measurement is opioid consumption.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- Female
- Target Recruitment
- 188
Inclusion Criteria
- Age 18 -69 years
- Gender . female
- ASA status 1-3
- Vaginal hysterectomy or laparoscopic hysterectomy
Exclusion Criteria
- Body mass Index over 35
- Diabetes Mellitus
- Liver disease
- Allergies to pharmaceuticals used in the Study
- Present use of opioids
- Vaginal prolapse
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description laparoscopy laparoscopy, laparoscopic hysterectomy Intervention: Procedure: laparoscopy
- Primary Outcome Measures
Name Time Method Postoperative consumption of an opioid (oxycodone) 20 hours the consumption of oxycodone will be monitored by recording the amount of the drug received via a commercially available patient controlled analgesia (PCA) pump
- Secondary Outcome Measures
Name Time Method NRS (numeral rating scale) of pain 20 hours NRS is evaluated frequently during the study period.
Trial Locations
- Locations (1)
Tampere University Hospital
🇫🇮Tampere, Finland