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NCT05121168 · ClinicalTrials.gov registry record · Phase 4

Continuous Erector Spinae Plane Blocks to Treat Pain Following Percutaneous Nephrolithotomy

A Phase 4 study of Pain, Acute Postoperative and Renal Stone, sponsored by University of California, San Diego.

Completed
Registry status
Phase 4
Development phase
50
Enrollment target
2
Study locations

NCT05121168: Completed Phase 4 study of Pain, Acute Postoperative and Renal Stone, sponsored by University of California, San Diego.

NCT05121168 is a Phase 4 study of Pain, Acute Postoperative and Renal Stone that has completed, run by University of California, San Diego. The registered enrollment target is 50 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (90% lower). The trial reports 2 study locations across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT05121168, a Phase 4 study of Pain, Acute Postoperative and Renal Stone, has completed, sponsored by University of California, San Diego.

COMPLETED
Registry status
Phase 4
Development phase
50 participants
Enrollment target
2
Study locations

Study Summary

This is a randomized, triple-masked, placebo-controlled parallel-arm human subjects clinical trial investigating the addition of a continuous erector spinae plane nerve block to a single-injection erector spinae plane block to provide postoperative analgesia following percutaneous nephrolithotomy. Participants will all receive a single-injection nerve block and perineural catheter insertion. Following surgery, participants will be randomly allocated to receive either perineural local anesthetic or normal saline until the second day following surgery.

Primary Outcome

The numeric rating scale is a 0-10 Likert scale measuring pain level with 0 = no pain and 10 = worst imaginable pain scale. To claim that the addition of an ambulatory continuous erector spinae plane block is superior to a single-injection block alone, at least one of the two primary outcomes must be superior while the other at least non-inferior.

Interventions

  • DRUG Active bupivacaine 0.25% via an erector spinae plane perineural catheter
  • DRUG Placebo normal saline via an erector spinae plane perineural catheter

Study Locations (2)

California

  • UC San Diego - San Diego
  • University of California, San Diego - San Diego

Trial Details

FieldValue
Enrollment Target 50 participants
Start Date 2022-03-16
Est. Completion 2025-11-08
Phase Phase 4
University of California, San Diego

775 total trials

What the finished NCT05121168 record still lists

NCT05121168 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 50 participants, a relatively small participant target, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (90% lower).

The record links to 2 conditions, with Pain, Acute Postoperative appearing as the primary indexed condition, and to 2 interventions - of which Active bupivacaine 0.25% via an erector spinae plane perineural catheter is the first listed.

NCT05121168 reports a single indexed study location in California.

Frequently Asked Questions

What is clinical trial NCT05121168 about?

NCT05121168 is a clinical study titled "Continuous Erector Spinae Plane Blocks to Treat Pain Following Percutaneous Nephrolithotomy". This is a randomized, triple-masked, placebo-controlled parallel-arm human subjects clinical trial investigating the addition of a continuous erector spinae plane nerve block to a single-injection erector spinae plane block to provide postoperative analgesia following percutaneous nephrolithotomy. P...

What is the current status of trial NCT05121168?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 50 participants. The study started on 2022-03-16. Estimated completion is 2025-11-08.

What conditions does trial NCT05121168 study?

This clinical trial studies the following conditions: Pain, Acute Postoperative, Renal Stone.

What interventions are being tested in trial NCT05121168?

The interventions under investigation include: Active bupivacaine 0.25% via an erector spinae plane perineural catheter (DRUG), Placebo normal saline via an erector spinae plane perineural catheter (DRUG).

Who is sponsoring clinical trial NCT05121168?

This trial is sponsored by University of California, San Diego, which has 775 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05121168 being conducted?

This trial has 2 study locations across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

How this trial's enrollment target compares

Where NCT05121168's enrollment target sits among peer trials

50 1255th of 2000 higher than 679 of 2,000 other Phase 4 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 4 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT05121168, the US trial registry maintained by the National Library of Medicine. NCT05121168 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.