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Study of two block in laproscopic pyeloplasty for post operative pain relief

Comparative study between quadratus lumborum versus transverse abdominis plane block in laparoscopic pyeloplasty for post-operative pain relief

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/12/048155
Enrollment
60
Registered
2022-12-15
Start date
Unknown
Completion date
Unknown
Last updated
2023-01-09

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

Conditions

Health Condition 1: 8- Other Procedures

Interventions

Intervention1: Transversus abdominis plane block (group A): Postoperative pain will be managed using transversus abdominis plane block using 20 ml of 0.25% Bupivacaine. Intervention2: Quadratus lumbor

Sponsors

Department of Anaesthesiology
Lead Sponsor
Department of Urology
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: Patients of either sex aged 18-65 years ASA grade I-II patients scheduled to undergo elective laparscopic pyeloplasty under GA

Exclusion criteria

Exclusion criteria: Patients not giving consent Local infection at site of block H/o allergy to study medications Patients taking α agonist / antagonist regular pain medication

Design outcomes

Primary

MeasureTime frame
Time for first rescue analgesic requirementTimepoint: After end of surgery at: 0 minutes, 30 minutes, 2 hours, 4 hours, 6 hours, 12 hours, 24 hours—

Secondary

MeasureTime frame
Visual Analogue scale for pain (ranging from 0 to 10, where 0 no pain and 10 maximum pain) will be evaluated postoperatively at 30 min and 2, 4, 6, 12, and 24 h postoperative Timepoint: 24hrs—

Countries

India

Contacts

Public ContactProf Dinesh Kaushal

King Georges Medical University Lucknow

dineshkaushal91@yahoo.com9839089242

Outcome results

None listed

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