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RECRUITING

A Multicenter Patient Registry on Outcomes From Cryoanalgesia of the Intercostal Nerves

NCT05110989 · View on ClinicalTrials.gov ↗

Study Summary

This is a retrospective and prospective, multicenter, observational patient registry to record outcomes from patients undergoing cryoablation of the intercostal nerves (cryoanalgesia) for post-operative pain management.

Conditions Studied

Interventions

  • DEVICE AtriCure Cryo Nerve Block (cryoNB) Device Family

Study Locations (6)

Florida

  • AdventHealth — Orlando

Michigan

  • Henry Ford Health Rochester Hospital — Rochester

Missouri

  • St. Luke's Hospital of Kansas City — Kansas City

New Hampshire

  • Elliot Hospital — Manchester

Ohio

  • The Christ Hospital — Cincinnati

Texas

  • Baylor College of Medicine — Houston

Trial Details

FieldValue
Enrollment Target 5,000 participants
Start Date 2018-06-29
Est. Completion 2040-01

Sponsor

AtriCure

13 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT05110989

The ClinicalTrials.gov registry entry for NCT05110989 describes a study currently listed as recruiting. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 5,000 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is AtriCure, which has 13 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Post Operative Pain appearing as the primary indexed condition, and to 1 intervention — of which AtriCure Cryo Nerve Block (cryoNB) Device Family is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT05110989 reports 6 study locations spanning 6 distinct geographic areas — top geographies include Florida, Michigan, Missouri. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT05110989 about?

NCT05110989 is a clinical study titled "A Multicenter Patient Registry on Outcomes From Cryoanalgesia of the Intercostal Nerves". This is a retrospective and prospective, multicenter, observational patient registry to record outcomes from patients undergoing cryoablation of the intercostal nerves (cryoanalgesia) for post-operative pain management.

What is the current status of trial NCT05110989?

This trial is currently recruiting. The enrollment target is 5,000 participants. The study started on 2018-06-29. Estimated completion is 2040-01.

What conditions does trial NCT05110989 study?

This clinical trial studies the following conditions: Post Operative Pain. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT05110989?

The interventions under investigation include: AtriCure Cryo Nerve Block (cryoNB) Device Family (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT05110989?

This trial is sponsored by AtriCure, which has 13 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT05110989 being conducted?

This trial has 6 study locations across Florida, Michigan, Missouri, New Hampshire, Ohio. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial