se of paracetamol and paracetamol & dexmedetomidine combination for reduction of analgesic requirement and reduction of nausea and vomiting after operation in laparoscopic surgery.
Phase 4
Completed
- Conditions
- Health Condition 1: N859- Noninflammatory disorder of uterus, unspecifiedHealth Condition 2: N859- Noninflammatory disorder of uterus, unspecified
- Registration Number
- CTRI/2022/08/045086
- Lead Sponsor
- Apollo Hospitals Bilaspur
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 104
Inclusion Criteria
1. ASA grade I and II
2. Scheduled for laparoscopic gynaecological surgery under general anesthesia
Exclusion Criteria
1.Known allergy to study drugs
2.Use of antiemetic drugs within 24 hrs of surgery
3.Morbid obesity(BMI >40)
4.Chronic use of opioids
5.Patients with hepatic,renal or cardiovascular dysfunction
6.Psychiatric patients
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method