Comparison of pain relief after two types of abdominal field blocks in caesarean cases
Not Applicable
- Conditions
- Health Condition 1: O80- Encounter for full-term uncomplicated delivery
- Registration Number
- CTRI/2019/12/022218
- Lead Sponsor
- niversity College of Medical Sciences Delhi
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Consenting patients with singleton pregnancy presenting for Caesarean section via pfannenstiel incision under subarachnoid block
Exclusion Criteria
1 Hypertensive disorders of pregnancy
2 Hemodynamically unstable patient
3 Body weight less than 50kg
4 History of allergy to local anaesthetic drug
5 Morbid Obesity
6 Chronic pain, recent use of analgesic drugs
or substance abuse
7 Inability to understand procedure and scale
used
8 Contraindication to regional anaesthesia
9 Any patient requiring general anaesthesia
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To determine and compare the duration of post-operative pain relief following TAP and TFP blockTimepoint: 48 hours
- Secondary Outcome Measures
Name Time Method 1 To determine and compare <br/ ><br> the rescue analgesic <br/ ><br> consumption over 48 hours <br/ ><br> in the two groups. <br/ ><br>2 To determine and compare <br/ ><br> pain scores (Numerical <br/ ><br> rating scores NRS static, <br/ ><br> dynamic and sleep) over 48 <br/ ><br> hours in two groups. <br/ ><br>3 To compare the patient <br/ ><br> satisfaction towards post <br/ ><br> operative pain management <br/ ><br> in the two groups by using <br/ ><br> American Pain Society <br/ ><br> Revised Patient Outcome <br/ ><br> Questionnaire <br/ ><br>4 To compare the side <br/ ><br> effects if any in the two <br/ ><br> groupsTimepoint: 48 hours