To compare effects of two heavy local anaesthetics in patients undergoing gynecological surgeries under spinal anaesthesia.
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2023/10/059198
- Lead Sponsor
- Department of Anaesthesia and Intensive Care
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Age group between 18-65 years
American Society of Anaesthesiologists (ASA) physical status I and II of either sex
BMI = 20 to = 35kg/m²
Duration of surgery upto 2-2.5 hours in gynecological surgeries (I.e Vaginal
hysterectomy, Cervical polypectomy, Tubal recanalisation, Myomectomy, Dilatation and
evacuation)
Pre- existing local infection at the site of subarachnoid block
Patients with coagulopathy and platelet disorders
Contraindication or allergy to study drugs
Patients having pain in any other area than the surgery site
Patients having sensory or motor problem in the lower limb
Patients who failed to understand the VAS scoring system
Pregnant and lactating women
Patients with current history of psychiatric illness, communication difficulties
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method