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Comparison of pain relief after two types of abdominal field blocks in caesarean cases

Efficacy of Ultrasound Guided Transversus Abdominis Plane Block versus Transversalis Fascia Plane Block for Postoperative Pain Relief in Caesarean section through Pfannensteil Incision - A Randomised Comparative Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/12/022218
Enrollment
50
Registered
2019-12-02
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: O80- Encounter for full-term uncomplicated delivery

Interventions

Intervention1: Transversalis Fascia Plane Block ( TFP): After completion of Caesarean section bilateral TFP block will be performed using 0.375% Ropivacaine Control Intervention1: Transversus Abdomini

Sponsors

University College of Medical Sciences Delhi
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Consenting patients with singleton pregnancy presenting for Caesarean section via pfannenstiel incision under subarachnoid block

Exclusion criteria

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

Design outcomes

Primary

MeasureTime frame
To determine and compare the duration of post-operative pain relief following TAP and TFP blockTimepoint: 48 hours—

Secondary

MeasureTime frame
1 To determine and compare the rescue analgesic consumption over 48 hours in the two groups. 2 To determine and compare pain scores (Numerical rating scores NRS static, dynamic and sleep) over 48 hours in two groups. 3 To compare the patient satisfaction towards post operative pain management in the two groups by using American Pain Society Revised Patient Outcome Questionnaire 4 To compare the side effects if any in the two groupsTimepoint: 48 hours—

Countries

India

Contacts

Public ContactDr Aman Yadav

University College of Medical Sciences and Guru Teg Bahadur Hospital

drzainabhaq@gmail.com9354346045

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026