Health Condition 1: null- patients undergoing orthopaedic upper extremity surgery
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1.Males and females between the age group 18-60 years. 2. ASA class I-II. 3. BMI 18.5-29.9. 4. Undergoing surgeries around elbow, forearm and hand.
Exclusion criteria
Exclusion criteria: 1.Patients refusal for block. 2.Patients having bleeding disorders. 3.Local infection at the site where needle for block is to be inserted. 4.Allergic to study drugs. 5.Patients of head injury, renal disease, liver disease and cardiac disease. 6.Patients in whom the block effect will be partial and will require supplementary anesthesia
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| â?¢To study and compare the duration of analgesia in three group of patients.Timepoint: duration of analgesia | — |
Secondary
| Measure | Time frame |
|---|---|
| â?¢To evaluate and compare the onset and duration of sensory and motor blockade with lignocaine with adrenaline (1: 200000) alone and with midazolam in two different doses. â?¢To find the optimal dose of midazolam as an adjunct for brachial plexus block and post-operative analgesia. â?¢To observe for side effects of midazolam, if any. Timepoint: .onset and duration of sensory and motor block | — |
Countries
India
Contacts
Dr Rajendra Prasad Government Medical College