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NCT05415384 · ClinicalTrials.gov registry record · NA
Randomized Control Trial, Cryoablation as an Adjunct to Surgical Stabilization of Rib Fractures
A NA study of Pain, Postoperative and Rib Fracture Multiple, sponsored by Wake Forest University Health Sciences.
- Recruiting
- Registry status
- NA
- Development phase
- 80
- Enrollment target
- 1
- Study location
NCT05415384: Recruiting NA study of Pain, Postoperative and Rib Fracture Multiple, sponsored by Wake Forest University Health Sciences.
NCT05415384 is a NA study of Pain, Postoperative and Rib Fracture Multiple that is actively recruiting participants, run by Wake Forest University Health Sciences. The registered enrollment target is 80 participants, below the 272-participant average among 113 other Pain, Postoperative trials with a reported enrollment target (71% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT05415384, a NA study of Pain, Postoperative and Rib Fracture Multiple, is actively recruiting participants, sponsored by Wake Forest University Health Sciences.
- RECRUITING
- Registry status
- NA
- Development phase
- 80 participants
- Enrollment target
- 1
- Study location
Study Summary
To determine if patients with intraoperative cryoablation have better analgesia results compared to the control group of Surgical Stabilization of Rib Fractures (SSRF) without cryoablation
Primary Outcome
To determine if patients with intraoperative cryoablation have better analgesia results compared to the control group of SSRF without cryoablation.
Conditions Studied
Interventions
- DEVICE Cryoablation of Intercostal Nerves
- PROCEDURE Standard surgical treatment of patients with multiple rib fractures
Study Locations (1)
North Carolina
- Wake Forest University Health Sciences - Winston-Salem
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 80 participants |
| Start Date | 2022-08-01 |
| Est. Completion | 2026-09 |
| Phase | NA |
What NCT05415384 shows while recruiting
NCT05415384 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 80 participants, a relatively small participant target, below the 272-participant average among 113 other Pain, Postoperative trials with a reported enrollment target (71% lower).
The record links to 2 conditions, with Pain, Postoperative appearing as the primary indexed condition, and to 2 interventions - of which Cryoablation of Intercostal Nerves is the first listed.
NCT05415384 reports a single indexed study location in North Carolina.
Frequently Asked Questions
What is clinical trial NCT05415384 about?
NCT05415384 is a clinical study titled "Randomized Control Trial, Cryoablation as an Adjunct to Surgical Stabilization of Rib Fractures". To determine if patients with intraoperative cryoablation have better analgesia results compared to the control group of Surgical Stabilization of Rib Fractures (SSRF) without cryoablation
What is the current status of trial NCT05415384?
This trial is currently recruiting. It is a NA study. The enrollment target is 80 participants. The study started on 2022-08-01. Estimated completion is 2026-09.
What conditions does trial NCT05415384 study?
This clinical trial studies the following conditions: Pain, Postoperative, Rib Fracture Multiple.
What interventions are being tested in trial NCT05415384?
The interventions under investigation include: Cryoablation of Intercostal Nerves (DEVICE), Standard surgical treatment of patients with multiple rib fractures (PROCEDURE).
Who is sponsoring clinical trial NCT05415384?
This trial is sponsored by Wake Forest University Health Sciences, which has 1,140 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT05415384 being conducted?
This trial has 1 study location across North Carolina. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Pain, Postoperative
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
Where NCT05415384's enrollment target sits among peer trials
80 56th of 113 higher than 53 of 113 other Pain, Postoperative trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Pain, Postoperative 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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