study to determine the efficacy of surgeon administered open wound TAP block versus standard anatomical TAP block for analgesia after cesarean delivery
- Conditions
- Health Condition 1: O00-O9A- Pregnancy, childbirth and the puerperium
- Registration Number
- CTRI/2021/12/038786
- Lead Sponsor
- Archana Mehra
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
1. Patient posted in Dr Susheela Tiwari Government Hospital for cesarean section
2. asa physical status II
Patient refusal for consent.
2.ASA grade III and IV.
3.History of allergy to proposed/used drugs in the study.
4.Patient with chronic pain history.
5.Patient with any Contraindication of spinal anesthesia.
6..Morbid obesity.
7.Local infection at the site of block administration.
Patient refusal for consent.
2.ASA grade III and IV.
3.History of allergy to proposed/used drugs in the study.
4.Patient with chronic pain history.
5.Patient with any Contraindication of spinal anesthesia.
6..Morbid obesity.
7.Local infection at the site of block administration.
Patient refusal for consent.
2.ASA grade III and IV.
3.History of allergy to proposed/used drugs in the study.
4.Patient with chronic pain history.
5.Patient with any Contraindication of spinal anesthesia.
6..Morbid obesity.
7.Local infection at the site of block administration.
1.Patient refusal for consent
2.ASA III and ASA IV
3.History of allergy to proposed/used drugs in the study
4.Patient with chronic pain history.
5.Patient with any Contraindication of spinal anesthesia.
6. Morbid obesity.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare the VAS at rest and in movement between the two groupsTimepoint: 24 hrs
- Secondary Outcome Measures
Name Time Method to compare the first request of analgesia between the two groups and to compare the total post operative rescue analgesiaTimepoint: 24 hours