Postoperative pain management in hysterectomy patient
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2024/08/071886
- Lead Sponsor
- Kasturba Medical College
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. Patients with benign gynaecologic conditions (fibroids, pelvic pain, uterine prolapse)
who are planned to undergo hysterectomy under spinal anaesthesia.
2. Female patients older than 18 years with ASA I or II.
Exclusion Criteria
1. Patients with chronic non-gynaecologic conditions (liver or pulmonary disease,
diabetes mellitus)
2. The history of use of psychotropic drugs (anti-depressants, neuroleptics, lithium) in
the last 1 year.
3. Those with Duloxetine allergy.
4. Patients using opioids for gynaecologic or non-gynaecologic conditions.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1. Quality of Recovery-40 <br/ ><br>questionnaire total score <br/ ><br>2. Visual Analogue scoreTimepoint: Both the respective Groups will be assessed Postoperatively at 6th, 12th and 24th hours after the surgery. <br/ ><br>
- Secondary Outcome Measures
Name Time Method 1. Opioid analgesic consumption <br/ ><br>doses (Fentanyl) <br/ ><br>2. Adverse EventsTimepoint: 1. Opioid analgesic consumption (fentanyl) <br/ ><br>doses 24 hours after surgery <br/ ><br>2. Adverse Events During stay <br/ ><br>in postoperative ward at 48 hours