Health Condition 1: S529- Unspecified fracture of forearm
Conditions
Interventions
Intervention1: Ropivacaine with clonidine: Patients who will receive 29ml ropivacaine 0.5% and 1ml clonidine(50mcg)
Control Intervention1: Ropivacaine with dexmedetomidine: Patient who will receive 29
Sponsors
Dr Sampurnanand Medical College
Eligibility
Inclusion 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
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
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. To compare the duration of analgesia,onset of sensory and motor block of 0.5% Ropivacaine combined with either Dexmedetomidine or Clonidine as adjuvants injected perineurally. 2. Number of Rescue analgesic given in 24 hours in both groups 3. Total dose of rescue medication consumption (tramadol and Diclofenac) in 24 hrs.Timepoint: Assessment of block quality by calculation of composite score of bromage scale and duration of analgesia was recorded by patient response. | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. NRS pain scores at rest (NRS-R) & at movement (passive/active) NRS-M of operated upper limb in first 24 hours. 2. Patient’s satisfaction score. 3. Any complications / adverse effects/side effects of block. 4. Any changes inNIBP,PR&SpO 2 in first 24 hours.Timepoint: Assessment of block quality by calculation of composite score of bromage scale and duration of analgesia was recorded by patient response. | — |
Countries
India
Contacts
Public ContactDr Anjali Singh
Dr S. N. Medical college, jodhpur
Outcome results
None listed