POST OP ANALGESIA IN CESAREAN SECTIO
Phase 3
Completed
- Conditions
- Health Condition 1: O908- Other complications of the puerperium, not elsewhere classified
- Registration Number
- CTRI/2023/06/054045
- Lead Sponsor
- Dr Benita Abraham
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 50
Inclusion Criteria
Undergoing cesarean section
Exclusion Criteria
Patient refusal to ESPB
presence of coagulopathy or bleeding disorder
bradycardia
cardiac conduction block
were administered ß-adrenergic antagonist or an antiplatelet agent
local infection at the injection site
hypersensitivity to local amide anesthetics or were hypersensitive or allergic to dexmedetomidine
central neuropathy
a body mass index >35 kg/m2
uncontrolled diabetes mellitus
significant cardiopulmonary disease, hepatic or renal failure or psychiatric disease.
Inability to give consent to the study
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Total analgesic consumption in the first 24 hours after surgeryTimepoint: Total analgesic consumption in the first 24 hours after surgery
- Secondary Outcome Measures
Name Time Method Incidence of bradycardiaTimepoint: Number;Incidence of hypotensionTimepoint: Number;Incidence of post operative nausea & vomittingTimepoint: Number;Time for first request to analgesiaTimepoint: Hours;Visual analog scale (VAS) for painTimepoint: 0 hour, 2 hours , 4hours, 6 hours , 8 hours, 12hours 24 hours & 48 hours