CTRI/2020/06/025823
Not yet recruiting
未知
â??A comparative study of safety and efficacy of 0.5%Ropivacaine combined with either Dexmedetomidine orClonidine as adjuvant ; given as USG guidedsupraclavicular brachial plexus block, in patientsundergoing elective upper limb orthopaedic surgery.â??
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Health Condition 1: S529- Unspecified fracture of forearm
- Sponsor
- Dr Sampurnanand Medical College
- Status
- Not yet recruiting
- Last Updated
- 4 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •ASA I \& II of body weight 30 to 80 kg, undergoing upperlimb orthopaedic surgery of less than two hours duration.
- •Free from any associated chronic systemic illness.
Exclusion Criteria
- •Uncooperative patient
- •Pregnant or lactating mother
- •Neurological deficit in operative limb with chronic pain or on long term analgesics
- •Patient having hypersensitivity or contraindication to Ropivacaine/ Dexmedetomidine/ Clonidine
- •Local pathology at the site of injection
- •All disability limiting the performance of block
Outcomes
Primary Outcomes
Not specified
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