Comparison between efficacy of combination of drugs with additives given for spinal anaesthesia.
Not Applicable
- Conditions
- Health Condition 1: L089- Local infection of the skin and subcutaneous tissue, unspecifiedHealth Condition 2: O- Medical and SurgicalHealth Condition 3: M958- Other specified acquired deformities of musculoskeletal systemHealth Condition 4: S729- Unspecified fracture of femurHealth Condition 5: S899- Unspecified injury of lower legHealth Condition 6: N23- Unspecified renal colic
- Registration Number
- CTRI/2021/05/033466
- Lead Sponsor
- Dr Prabhakar Kore hospital and medical research centre
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients undergoing elective lower abdominal surgery falling under ASA Grade 1 or 2, weighing between 50 to 70 kgs and height between 150 to 175 Cms
Exclusion Criteria
Hypovolemic patients, spinal deformity, uncooperative patients, contraindications to spinal anaesthesia, pregnant patients, pre existing neurologic deficits and those not willing to be part of trial.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Time taken to achieve sensory blockade and motor blockade using modified bromage score. And duration of sensory and motor blockade.Timepoint: From the time of giving spinal anaesthesia to 10 minutes duration and post surgery 3 hour duration to record duration of block.
- Secondary Outcome Measures
Name Time Method evel of Sedation using modified Wilson score and bradycardia.Timepoint: From modified Wilson scale 1 to 4 and bradycardia seen during surgery.