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A study to compare the duration of post operative pain relief after administration of ultrasound-guided Quadratus Lumborum block and Transversus Abdominis Plane block in patients undergoing Cesarean Section.

Ultrasound-Guided Quadratus Lumborum Block Versus Transversus Abdominis Plane Block for post operative analgesia in patients undergoing Lower Segment Cesarean Section: A randomized comparative study - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/02/062925
Enrollment
60
Registered
2024-02-20
Start date
Unknown
Completion date
Unknown
Last updated
2024-03-04

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

Conditions

Health Condition 1: O94- Sequelae of complication of pregnancy, childbirth, and the puerperium

Interventions

Intervention1: Transversus Abdominis Plane block: Ultrasound-guided Transversus Abdominis Plane Block with 20 ml of 0.25% bupivacaine on each side (maximum dose- 2 mg/kg). The nerve block will be admi

Sponsors

Department of Anaesthesiology
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients posted for Lower Segment Cesarean Section under spinal anaesthesia

Exclusion criteria

Exclusion criteria: 1. ASA physical status III and IV 2. Known allergy to local anaesthetic drugs 3. Coagulation disorders 4. Local infection at the site of block

Design outcomes

Primary

MeasureTime frame
Duration of postoperative analgesia (time at which first rescue analgesic required)Timepoint: time at which first rescue analgesic required, that is, Numeric Rating Score more than 4—

Secondary

MeasureTime frame
Adverse effects related to the block- Local hematoma or infection, lower limb weakness, hemodynamic variations .Timepoint: 24 hrs;Maternal satisfactionTimepoint: 24 hrs;Time taken for administration of block (time taken from insertion of needle to administration of drug)Timepoint: time taken from insertion of needle to administration of drug;Total dose of rescue analgesic required in first 24hrs postoperativelyTimepoint: 24 hrs—

Countries

India

Contacts

Public ContactDr Sonali Samant

Atal Bihari Vajpayee Institute of Medical Sciences, Dr Ram Manohar Lohia Hospital, New Delhi

nehaguptadeuri@gmail.com9899567234

Outcome results

None listed

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