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Improving pain management after laparascopic surgery for kidney stones

Ultrasoundguided Transmuscular Quadratus Lumborum(TQL) block for percutaneous nephrolithotomy (PNL) - a randomized controlled trial

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
EU CTR
Registry ID
EUCTR2015-004770-16-DK
Enrollment
60
Registered
2015-11-25
Start date
2016-01-04
Completion date
Unknown
Last updated
2018-02-19

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

Conditions

The postoperative pain after percutaneous nephrolithotomy(PNL) operation. Our one year retrospective study of patients treated with PNL, revealed that, 71% of all patients undergoing PNL operation had a NRS score 3-10 in the PACU, and they needed substantial amounts of opioids to alleviate the postoperative pain MedDRA version: 18.1 Level: LLT Classification code 10038286 Term: Regional nerve block System Organ Class: 100000004865

Interventions

Sponsors

Jens Børglum
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: PErforming elective PNL in general anesthesia, Received written and oral information about the study and sign the infromed consent form of participating the study, ASA 1-3 Are the trial subjects under 18? no Number of subjects for this age range: F.1.2 Adults (18-64 years) yes F.1.2.1 Number of subjects for this age range 45 F.1.3 Elderly (>=65 years) yes F.1.3.1 Number of subjects for this age range 15

Exclusion criteria

Exclusion criteria: Unabel to understand Danish in written or spoken language, Unable to Cooperato to the procedure, daily use of opioids Known abouse of alcohol ore medication Diffcuilities in visualizing nerve ore muscle structure necessary for performing the block Pregnant women

Design outcomes

Primary

MeasureTime frame
Main Objective: To demonstrate whether a unilateral USG TQL block can reduce opioid consumption with clinical significance in PNL-patients.;Secondary Objective: not applicable;Primary end point(s): total doses of Opioid during the first 6 postoperative hours;Timepoint(s) of evaluation of this end point: 6 hours

Secondary

MeasureTime frame
Secondary end point(s): Total dose of opioids during the first 24 hours,NRS (0-10) pain scores at rest, time in recovery, time to ambulation, total Length of stay;Timepoint(s) of evaluation of this end point: 24 hours

Countries

Denmark

Contacts

Public ContactJens Børglum

Dept of Anest. Copenhagen University Hospital - Roskilde

jedn@regionsjaelland.dk+4530700120

Outcome results

None listed

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