Efficacy of Trans Abdominis Plane Block for Post Cesarean Delivery Analgesia

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Clinical Phase

NA

Total Enrollment

100 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-04-01

Study Completion Date

2024-08-30

Brief Summary

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Relief from pain is part of the fundamental human right to health. (1) However, available evidence indicates an increasingly detailed understanding of the pathophysiology of pain and general inadequacy of its treatment.

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Detailed Description

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Background: Relief from pain is part of the fundamental human right to health. (1) However, available evidence indicates an increasingly detailed understanding of the pathophysiology of pain and general inadequacy of its treatment.

Rationale: Assessment and Improving the Pain Management Modality

Study objectives: In this study, determined the efficacy of TAP block in patients undergoing cesarean section.

Methods:

This study is a cross-sectional study. It is a multi-centric study as it was conducted in different Governmental hospitals.

Conditions

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Analgesia

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Group A,

women who received TAP block.

Group Type EXPERIMENTAL

TAP block

Intervention Type PROCEDURE

Women will receive TAP block.

Group B

Received Usual modality of analgesics (Paracetamol, Tramadol, and Pethidine).

Group Type ACTIVE_COMPARATOR

TAP block

Intervention Type PROCEDURE

Women will receive TAP block.

Interventions

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TAP block

Women will receive TAP block.

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

1. Age: 20-50 years
2. Patients of \>50 kg or \<100 kg weight.
3. Urgency: Elective, Emergent and Urgent cases

Exclusion Criteria

1. Patients of \<50 kg or \>100 kg weight
2. Any contraindication to any of anesthesia medications
3. Patient unable to understand numeric rating scale (NRS)

Minimum Eligible Age

18 Years

Maximum Eligible Age

50 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No