Comparison of Fentanyl and Buprenorphine administered by different routes on spinal anesthesia
Phase 4
Completed
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2019/08/020760
- Lead Sponsor
- Sri muthukumaran medical colle hospital and research institute
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
60-70kg weight
170-180cms height
asa I, II
posted for elective perineal surgery
Exclusion Criteria
Patients with contraindications to narcotics and spinal anesthesia
Patient refusal
Haemorrhagic disorders
Local infection
Severe hypertension
Spinal deformity
Raised intracranial tension
Known hypersensitivity to local anaesthetic drug
Autonomic neuropathy
COPD
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method post operative analgesiaTimepoint: 0-24 h post operative period
- Secondary Outcome Measures
Name Time Method post operative complcations-Shivering <br/ ><br>Nausea, Vomiting <br/ ><br>Respiratory Depression <br/ ><br>Pruritis <br/ ><br>Sedation <br/ ><br>Timepoint: intraopErative and postoperative period