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EFFICACY OF QUADRATUS LUMBORUM BLOCK VERSUS TRANSVERSUS ABDOMINIS BLOCK FOR PAIN RELIEF AFTER CESAREAN DELIVERY: A RANDOMISED COMPARATIVE STUDY

EFFICACY OF QUADRATUS LUMBORUM BLOCK VERSUS TRANSVERSUS ABDOMINIS PLANE BLOCK FOR POSTOPERATIVE ANALGESIA AFTER CESAREAN SECTION: A PROSPECTIVE RANDOMISED COMPARATIVE STUDY - nil

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/02/080310
Enrollment
60
Registered
2025-02-10
Start date
Unknown
Completion date
Unknown
Last updated
2025-03-03

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

Conditions

Health Condition 1: O998- Other specified diseases and conditions complicating pregnancy, childbirth and the puerperium

Interventions

Intervention1: Quadratus lumborum block: in this patient will be positioned in lateral decubitus position. r all aseptic and antiseptic precaution, a curvilinear low-frequency ultrasound probe will be

Sponsors

Medical college Baroda
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Age group of 20-40 years female posted for elective caesarean section under spinal anesthesia. 2.Normal singleton pregnancy with a gestation of at least 37 weeks. 3.ASA-II patients 4.Patient able to give verbal and informed consent. 5.Patient able to understand VAS regarding assessment of pain

Exclusion criteria

Exclusion criteria: Patient refusal. Allergy to local anaesthetics. Patient with local site infection. Patient with coagulopathy disorder. Patient with uncontrolled cardiac,renal, respiratory, neurological conditions. Any patient requiring general anesthesia at any point of time.

Design outcomes

Primary

MeasureTime frame
Time to first rescue analgesia (duration of analgesia in minutes)Timepoint: 48hrs

Secondary

MeasureTime frame
Secondary objectives: 1.To evaluate the post operative analgesia using visual analogue scale (VAS) measured at rest and on movement. 2.Total requirement of analgesic drugs in first 48 hours (in mg) 3.Hemodynamic parameters 4.Complications associated with the block. Timepoint: 48hrs

Countries

India

Contacts

Public ContactDr Ayushi chaudhary

medical college baroda

nimishabrahmbhatt7@gmail.com8160364508

Outcome results

None listed

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