A comparison of two treatment modalities for postoperative analgesia in lower limb surgeries
Not Applicable
- Conditions
- Health Condition 1: null- patients undergoing lower limb surgeries
- Registration Number
- CTRI/2018/04/013214
- Lead Sponsor
- Sri Guru Ram Das Medical institute of sciences and research
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
ASA grade 1 and 2
- patients undergoing lower limb surgeries
Exclusion Criteria
- ASA grade III and IV
- Patientâ??s refusal to participate in the study
- Contraindications to regional anesthesia such
as local infections/sepsis at
the site of lumbar puncture, space occupying
lesions of the brain,
anatomical disorders of spine, shock, etc
- Hypersensitivity to study drugs
- Neurological disorders
- Coagulation disorders
- Pregnant women
- History of opioid dependence
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method duration of postoperative analgesiaTimepoint: duration of postoperative analgesia
- Secondary Outcome Measures
Name Time Method a.Onset, duration of sensory & motor blockade and to evaluate the <br/ ><br>hemodynamic changes <br/ ><br>b. Complications related to procedures, side effects associated with <br/ ><br>study drugs and sedation scoreTimepoint: a. to evaluate onset, duration of sensory and motor blockade till 24 hours after the surgery <br/ ><br>b.intraoperative and postoperative hemodynamic stability upto 24 hours after surgery <br/ ><br>c. complications related to procedure, side effects and sedation score upto 24 hours after surgery.