Skip to content

Comparison of two regional block techniques in patients undergoing cesarean section

Comparison of combined Transversus Abdominis Plane block and Transversalis Fascia Plane block versus transversus abdominis plane block in patients undergoing cesarean section: a randomized controlled trial - NIL

Status
Active, not recruiting
Phases
Phase 1Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/06/088143
Enrollment
130
Registered
2025-06-03
Start date
Unknown
Completion date
Unknown
Last updated
2025-06-24

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Combined Transversus Abdominis Plane block and Transversalis Fascia Plane block: Ultrasound guided bilateral transversalis fascia plane block will be provided with 15 ml of 0.25% isobar

Sponsors

Jawaharlal Institute of Postgraduate Medical Education and Research
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Parturient undergoing elective and emergency caesarean delivery performed using a Pfannenstiel incision under spinal anesthesia 2. American Society of Anesthesiologists physical status (ASA-PS) II 3. Body mass index (BMI) of 18 35 kg/m2.

Exclusion criteria

Exclusion criteria: 1. Patient refusal 2. NICE Category 1 Cesarean section 3. History of local anesthetics (LA) allergy 4. Coagulopathy 5. Local site infection 6. Preoperative use of analgesic drugs 7. Requirement of general anesthesia

Design outcomes

Primary

MeasureTime frame
To compare the total opioid consumption following TAP block and combined TAP and TFP block in patients undergoing cesarean section under spinal anesthesiaTimepoint: 24 hours post-intervention

Secondary

MeasureTime frame
VAS scores at rest and movementTimepoint: 0, 2, 4, 8,12 and 24 hours post-intervention;Duration of analgesiaTimepoint: ;Ease of block performanceTimepoint: ;Obstetric quality of recovery Score 11 (ObsQoR-11)Timepoint: 24 hours post-intervention

Countries

India

Contacts

Public ContactYaal Elango

Jawaharlal Institute of Postgraduate Medical Education and Research

drvstalin@gmail.com9786397762

Outcome results

None listed

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