A study to compare the effectiveness and safety of different doses of a drug clonidine when used along with a drug bupivacaine in spinal anesthesia
Phase 1
- Conditions
- Health Condition 1: S729- Unspecified fracture of femurHealth Condition 2: S929- Unspecified fracture of foot and toeHealth Condition 3: S829- Unspecified fracture of lower leg
- Registration Number
- CTRI/2019/05/019341
- Lead Sponsor
- J J hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
ASA I or II normotensive patients undergoing elective orthopaedic surgery
Exclusion Criteria
ASA III & above, patients with cardiovascular, renal, liver dysfunction, allergy to clonidine or bupivacaine, short height ( <130cm), obese(BMI > 30kg/m2) or with contraindication to spinal
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Duration of analgesia/sensory block <br/ ><br>Block height <br/ ><br>Hemodynamic variations-pulse, MAP <br/ ><br>ComplicationsTimepoint: 1year
- Secondary Outcome Measures
Name Time Method Hemodynamic effects-pulse and MAP <br/ ><br>ComplicationsTimepoint: 1 year