Comparing duration of two drugs clonidine and fentanyl along with bupivacaine for anaesthesia
Phase 4
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2024/02/063093
- Lead Sponsor
- Dr Santhosh M C B
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
ASA grade I and II
Patients willing to give informed consent to participate
Exclusion Criteria
Patients allergic to study anaesthetic drugs
Patients shorter than 150cm and taller than 180cm height
Patients with BMI more than 25kg per square meter
Patients on long term treatment with any opioids for chronic pain
Patients taking alpha receptor antagonists Calcium channel blockers Angiotension converting enzyme inhibitors or any any kind of analgesics
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare the sensory and motor characterstics between fentanyl and clonidine as adjuvant to intrathecal hyperbaric bupivacaine for infraumbilical surgeriesTimepoint: 12 hours
- Secondary Outcome Measures
Name Time Method To compare cardiorespiratory changes and adverse events between the groupsTimepoint: 12 hours