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Three regional anaesthesia techniques for post cesarean section analgesia

Not Applicable
Conditions
Health Condition 1: O749- Complication of anesthesia duringlabor and delivery, unspecifiedHealth Condition 2: O758- Other specified complications of labor and delivery
Registration Number
CTRI/2021/02/031289
Lead Sponsor
Dr Aman Malawat
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1. Patient with ASA Class II, III

2. Normal singleton pregnancy with a gestation of at least 37 weeks

3. Patientâ??s written and informed consent

Exclusion Criteria

1. Patient with ASA Class IV & V

2. Patient refusal

3. Local infection at the site of injection

4. Allergy to study medications

5. Anatomic abnormalities

6. Systemic anticoagulation or coagulopathy

7. Inability to comprehend or participate in pain scoring system

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To compare time of first rescue analgesic needed.Timepoint: baseline
Secondary Outcome Measures
NameTimeMethod
To compare severity of postoperative pain via visual analogue pain scale at rest (VASR) and with movement (dynamic)Timepoint: 48 hours;To compare the total cumulative dose of analgesic needed in first 48 hours after surgery.Timepoint: 48 hours
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