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Observing effect of a ultrasound guided muscle plane (quadratus Lumborum) block on post operative pain in patients undergoing Laproscopic pyeloplasty operation.

Assessing the efficacy of ultrasound guided posterior quadratus lumborum block for post operative analgesia in patients undergoing laparoscopic pyeloplasty.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2017/10/010281
Enrollment
60
Registered
2017-10-31
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: null- Patients undergoing Laproscopic pyeloplasty surgery

Interventions

Intervention1: Ultrasound guided quadratus lumborum block on side of operation: o.5% ropivacaine infiltrated in posterior quadratus lumborum plane after completion of surgery Control Intervention1: Po

Sponsors

none
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. ASA class I/II Patients undergoing Laproscopic pyeloplasty

Exclusion criteria

Exclusion criteria: 1. Refusal to participate in the study 2. Patients allergic to local anaesthetics 3. Coagulopathy or thrombocytopenia 4. Infection at the proposal site of injection 5. Known cardio-respiratory impairment 6. Morbid obesity. • Age 60 yrs • ASA 3 or higher

Design outcomes

Primary

MeasureTime frame
Static and dynamic VAS will be assessed for both the groups on shifting to post operative area, 2hrs, 6hrs, 12hrs and 24hrs postoperatively. Timepoint: 1. 30minutes after shifting patient to post operative area. 2. 2hrs after completion of surgery, 3. 6hrs after completion of surgery 4. 12hrs after completion of surgery 5. 24hrs postoperatively.

Secondary

MeasureTime frame
1. Requirement of rescue analgesics in 24 hour duration will be noted. Timepoint: 24 hours postoperatively;3. Side effects like hypotension or nausea if anyTimepoint: 1. 30 minutes after shifting to postoperative area. 2. 2 hours postoperatively 3. 6 hours postoperatively 4. 6 hours postoperatively 5. 12 hours postoperatively 6. 24 hours postoperatively

Countries

India

Contacts

Public ContactDivya Srivastava

SGPGIMs, Lucknow

dr.divshri@gmail.com7839098150

Outcome results

None listed

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