A comparative study of nalbuphine and fentanyl as additives to bupivacaine in spinal anaesthesia in patients undergoing TURP surgery
Phase 1
Completed
- Conditions
- Health Condition 1: null- ASA I AND II PATIENTS UNDERGOING ELECTIVE TURP SURGERIESHealth Condition 2: N401- Benign prostatic hyperplasia withlower urinary tract symptoms
- Registration Number
- CTRI/2019/09/021013
- Lead Sponsor
- department of anaesthesia dayanand medical college and hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 60
Inclusion Criteria
ASA grade I and II
Exclusion Criteria
1. ASA grade III or more
2. Patients refusal for subarachnoid block.
3. Patients on anticoagulant medication.
4. History of anaphylaxis to local anaesthetics.
5. Infection at site of injection.
6. patient with spinal deformities.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1. onset and duration of sensory block level. <br/ ><br>2. onset and duration of motor block level. <br/ ><br>3. evaluating haemodynamic parameters. <br/ ><br>Timepoint: onset of sensory and motor block level and haemodynamic parameters to be evaluated every 5 minutes for first 15 minutes and then every 15 minutes for 90 minutes intraoperatively. Duration of sensory and motor block assessed for the next 6hours and hemodynamic paramerters for the next 24 hours in the postoperative period. <br/ ><br>
- Secondary Outcome Measures
Name Time Method 1. Duration of post operative analgesia. <br/ ><br>2. Side effect profile with each drug. <br/ ><br>Timepoint: duration of postoperative analgesia to be recorded from the point of spinal injection till the patient first demands rescue analgesia. <br/ ><br>side effects to be noted both intraoperatively as well as postoperatively.