A comparative study of spinal drug with and without adjuvant in patients undergoing below umbilical surgeries
Phase 2
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2024/04/065142
- Lead Sponsor
- Bangalore medical college and research institute
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. Patient who is willing to participate in the study 2. Patients undergoing infraumbilical surgeries 3. Patients belonging to Americal Society of Anaesthesiologist class 1, 2 and 3
4. Duration of surgery less than 2 hours
Exclusion Criteria
1. Patient refusing to participate in the study
2. Patients with any contraindications for neuraxial blockade 3. Allergy to the study drug 4. Cardiogenic or hypovolemic shock 5. Respiratory insufficiency
6. Morbidly obese
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The postoperative analgesic efficacy of subarachnoid block by visual analog scoreTimepoint: Postoperative analgesic efficacy assessed over 24 hours by visual analog score
- Secondary Outcome Measures
Name Time Method Hemodynamic parameters <br/ ><br>Adverse effectsTimepoint: 24 hours