Pain Insensitivity, Congenital Clinical Trial
Official title:
Comparative Evaluation of Newer Congeners i.e. Levobupivacaine and Ropivacaine With Bupivacaine, in Lumbar Epidural Anaesthesia for Hip Surgeries
This study compares the clinical efficacy of newer local anaesthetic drugs Levobupivacaine and Ropivacaine with Bupivacaine in lumbar epidural anaesthesia for hip surgeries.
Status | Completed |
Enrollment | 90 |
Est. completion date | September 2014 |
Est. primary completion date | August 2014 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Both |
Age group | 18 Years to 60 Years |
Eligibility |
Inclusion Criteria: - ASA Grade I and II patients of either sex - Age 18-60 years - Undergoing various hip surgeries under lumbar epidural anesthesia Exclusion Criteria: - Refusal for epidural - ASA-III&IV - Head injury - Psychiatric disease - Known allergic to test drugs - Major systemic disease - Any analgesia with in past 24 hours |
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver), Primary Purpose: Supportive Care
Country | Name | City | State |
---|---|---|---|
India | Government Medical College | Haldwani | Uttarakhand |
Lead Sponsor | Collaborator |
---|---|
Government Medical College, Haldwani |
India,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Onset of sensory block | Time to achieve sensory block up to tenth thoracic dermatome | 30 minutes | No |
Secondary | Time for 2 segment regression of sensory block | Time for regression of sensory block 2 segments lower than maximum blocked dermatome | 90 minutes | No |
Secondary | Time to achieve maximum motor block | Time to achieve motor block of modified Bromage score | 45 minutes | No |
Status | Clinical Trial | Phase | |
---|---|---|---|
Not yet recruiting |
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