Compare the pain releif benefit of Ultrasound guided abdominal plane nerve block and standard pain releief technique in patients following cesarean delivery and its relation with OXTR gene
Phase 4
Completed
- Conditions
- Health Condition 1: O80- Encounter for full-term uncomplicated delivery
- Registration Number
- CTRI/2020/01/022813
- Lead Sponsor
- niversity College Of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 60
Inclusion Criteria
Patients of ASA grade I or II undergoing lower segment caesarean section with pfannenstiel incision under subarachnoid block
Exclusion Criteria
Patients having other causes of chronic pain,Patients having cognitive dysfunction or inability to comprehend various questionnaires, Patients having chronic neurological disorders/substance abuse,body mass index (BMI) > 40 kg/m2
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To determine and compare the time to first request of analgesia between the two groupsTimepoint: The Time to first request of analgesia will be measured from completion of the intervention i.e. wound infiltration or abdominal plane block following the completion of surgery till the patients first demand for analgesia
- Secondary Outcome Measures
Name Time Method RS pain score at rest and movement, <br/ ><br>Total consumption of diclofenac in 24 hours, Pain detect questionnaire (PDQ), NPSI scores, SF-12 score, <br/ ><br>Incidence of CPSPTimepoint: Incidence of CPSP at the end of 14th week and rest all parameters at the end of 1st, 6th and 12th, 24th hour and then at the end of 6th week, 10th week, and 14th week.