Study will be done on patients coming for elective lower abdominal surgeries and effects of four different doses of dexmedetomidine with hyperbaric ropivacaine in spinal anaesthesia will be compared
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2024/07/070283
- Lead Sponsor
- Simran Naval
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
All ASA Grade 1 and 2, patients scheduled for elective lower abdominal surgery under subarachnoid block
Exclusion Criteria
Patients with hypertension, diabetes, spinal deformity, coagulation disorder, drug allergy, cardiovascular , respiratory or neurological disorders, pregnant patients, height less than 140cm, BMI more than 30kg per meter square, impaired liver and renal function tests, ASA Grade 3, 4, local skin infections
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1.To asses onset and duration of sensory blockade from the time of drug adminitration <br/ ><br>2. Maximum sensory level achieved and time taken for it <br/ ><br>3.Time taken for 2 segment sensory regression <br/ ><br>4. Onset and duration of motor blockade <br/ ><br>5. Total duration of post op analgesiaTimepoint: 1.To asses onset and duration of sensory blockade from the time of administration of drug <br/ ><br>2. Maximum sensory level achieved and time taken for it <br/ ><br>3.Time taken for 2 segment sensory regression <br/ ><br>4. Onset and duration of motor blockade <br/ ><br>5. Total duration of post op analgesia every hour till time of rescue analgesia. <br/ ><br>Every outcome assessed every 30 seconds till 5 minutes, every 1 minuthe till next 10 minutes every 5 minutes till end of surgery
- Secondary Outcome Measures
Name Time Method Changes in hemodynamic parameters and adverse effectsTimepoint: 24 hours after spinal anaesthsia