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NCT05330611 · ClinicalTrials.gov registry record · NA

Treatment of Adult Traumatic Rib Fractures With Percutaneous Cryoneurolysis

A NA study, sponsored by Stanford University.

Completed
Registry status
NA
Development phase
43
Enrollment target

NCT05330611: Completed NA study, sponsored by Stanford University.

NCT05330611 is a NA study that has completed, run by Stanford University. The registered enrollment target is 43 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

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The verdict

NCT05330611, a NA study, has completed, sponsored by Stanford University.

COMPLETED
Registry status
NA
Development phase
43 participants
Enrollment target

Study Summary

The purpose of this research study is to examine the effectiveness of using the Iovera Smart Time 190, for ultrasound-guided cryoneurolysis, in trauma patients 18-64 years old with rib fractures that are not candidates for surgical stabilization. This will offer patients the benefits of cryoneurolysis of the intercostal nerves, thereby providing short and long term pain control while their ribs heal. The Iovera Smart Tip 190 is FDA approved for cryoneurolysis.

Primary Outcome

Patients will be asked to verbalize their numeric pain score, measured on a scale of 0 to 10, with 0 being no pain and 10 being the worst pain. Daily numeric pain score is collected on the day the patient is discharged from the hospital.

Interventions

  • OTHER Standard of Care
  • DEVICE Cryoneurolysis of Intercostal Nerves

Trial Details

FieldValue
Enrollment Target 43 participants
Start Date 2023-02-21
Est. Completion 2026-02-02
Phase NA
Stanford University

1,744 total trials

What the finished NCT05330611 record still lists

NCT05330611 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 43 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower).

The record links to 0 conditions, and to 2 interventions - of which Standard of Care is the first listed.

NCT05330611 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT05330611 about?

NCT05330611 is a clinical study titled "Treatment of Adult Traumatic Rib Fractures With Percutaneous Cryoneurolysis". The purpose of this research study is to examine the effectiveness of using the Iovera Smart Time 190, for ultrasound-guided cryoneurolysis, in trauma patients 18-64 years old with rib fractures that are not candidates for surgical stabilization. This will offer patients the benefits of cryoneurolys...

What is the current status of trial NCT05330611?

This trial is currently completed. It is a NA study. The enrollment target is 43 participants. The study started on 2023-02-21. Estimated completion is 2026-02-02.

What interventions are being tested in trial NCT05330611?

The interventions under investigation include: Standard of Care (OTHER), Cryoneurolysis of Intercostal Nerves (DEVICE).

Who is sponsoring clinical trial NCT05330611?

This trial is sponsored by Stanford University, which has 1,744 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT05330611's enrollment target sits among peer trials

43 1435th of 2000 higher than 565 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA 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 NCT05330611, the US trial registry maintained by the National Library of Medicine. NCT05330611 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.