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A clinical trial to compare two different types of abdominal wall blocks in providing post-operative pain relief after cesarean section

Comparison of ultrasound guided transversalis fascia and transversus abdominis plane blocks for post-operative analgesia following lower segment cesarean section- A double blinded randomized control trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/06/034221
Enrollment
90
Registered
2021-06-14
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: 1- Obstetrics

Interventions

Intervention1: Transversus Abdominis plane block: Transversus Abdominis plane block will be given at the end of cesarean section with 20 ml of 0.25 % bupivacaine on either side of the abdomen Interven

Sponsors

Mahatma Gandhi Medical college and Research Institute
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Age 18 to 45 years, ASA II and III patients, BMI- 18-35 kg/m2

Exclusion criteria

Exclusion criteria: Allergy to local anaesthetic drugs, seizure disorder, if any intra-operative surgical complications, Prolonged duration of labour, if cesarean section is done under general anaesthesia

Design outcomes

Primary

MeasureTime frame
Assess the static and dynamic pain scores post-operativelyTimepoint: Static and dynamic pain scores will be assessed post-operatively for 24 hours at regular time intervals by asking the patient to flex their legs and by turning to one side

Secondary

MeasureTime frame
Assessment of block dynamicsTimepoint: Loss of sensation to touch and cold will be assessed from T10 to L4 dermatomal levels;Measurement of 24 hour cumulative rescue analgesic consumptionTimepoint: After administering the first analgesic, even after 30 minutes if the pain continues to persist then the second rescue analgesic will be administered and the 24 hour cumulative analgesic consumption will be noted;Time to first analgesic requirementTimepoint: Patients will be given analgesic when they give a pain score of more than 3 The time from when the block was given to the time when the first analgesic is given will be noted as the duration of analgesia

Countries

India

Contacts

Public ContactR SRIPRIYA

MAHATMA GANDHI MEDICAL COLLEGE AND RESEARCH INSTITUTE SBV UNIVERSITY

docsripriya@gmail.com9365815939

Outcome results

None listed

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