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NCT03111381 · ClinicalTrials.gov registry record · Phase 2

Toradol to Reduce Ureteroscopic Symptoms Trial

A Phase 2 study, sponsored by Yale University.

Completed
Registry status
Phase 2
Development phase
94
Enrollment target

NCT03111381: Completed Phase 2 study, sponsored by Yale University.

NCT03111381 is a Phase 2 study that has completed, run by Yale University. The registered enrollment target is 94 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (29% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03111381, a Phase 2 study, has completed, sponsored by Yale University.

COMPLETED
Registry status
Phase 2
Development phase
94 participants
Enrollment target

Study Summary

Double blinded randomized controlled clinical trial to assess the impact of intraoperative Toradol on post-operative pain scores for patients undergoing ureteroscopy for urinary stone management.

Primary Outcome

Once the patient is at home, they will fill out a validated visual analog pain scale to rate their pain. This will be filled out once a day for a total of 7 days following the procedure. This is total morphine equivalent use. The range is 0 to infinity. Higher scores are equated to worse pain. The units are "ME" or morphine equivalents.

Interventions

  • DRUG Toradol

Trial Details

FieldValue
Enrollment Target 94 participants
Start Date 2017-08-01
Est. Completion 2020-06-01
Phase Phase 2
Yale University

1,492 total trials

What the finished NCT03111381 record still lists

NCT03111381 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 94 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (29% lower).

The record links to 0 conditions, and to 1 intervention - of which Toradol is the first listed.

NCT03111381 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03111381 about?

NCT03111381 is a clinical study titled "Toradol to Reduce Ureteroscopic Symptoms Trial". Double blinded randomized controlled clinical trial to assess the impact of intraoperative Toradol on post-operative pain scores for patients undergoing ureteroscopy for urinary stone management.

What is the current status of trial NCT03111381?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 94 participants. The study started on 2017-08-01. Estimated completion is 2020-06-01.

What interventions are being tested in trial NCT03111381?

The interventions under investigation include: Toradol (DRUG).

Who is sponsoring clinical trial NCT03111381?

This trial is sponsored by Yale University, which has 1,492 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03111381's enrollment target sits among peer trials

94 764th of 2000 higher than 1,235 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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 NCT03111381, the US trial registry maintained by the National Library of Medicine. NCT03111381 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.