CTRI/2019/05/019341
Not yet recruiting
Phase 1
A prospective randomized controlled trial to compare the efficacy and safety of different doses of clonidine when used as an adjuvant to intrathecal bupivacaine
J J hospital0 sites0 target enrollmentTBD
Overview
- Phase
- Phase 1
- Intervention
- Not specified
- 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
- Sponsor
- J J hospital
- Status
- Not yet recruiting
- Last Updated
- 4 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
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
Outcomes
Primary Outcomes
Not specified
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