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Intercostal Nerve Cryotherapy in Patients Undergoing Minimally Invasive Pulmonary Resection

StatusActive, Not Recruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗
Record status
This record was last updated February 13, 2026 (before its estimated March 20, 2026 completion). Its status may not reflect the trial's current state.

Record History

  1. Primary completion date: Jan 31, 2025 to Mar 20, 2026
    • Study completion date: Jul 7, 2025 to Mar 20, 2026
    v5
  2. Trial status: Recruiting to Active, Not Recruiting
    • Primary completion date: Dec 15, 2024 to Jan 31, 2025
    • Site details revised
    v4
  3. Primary completion date: Oct 7, 2023 to Dec 15, 2024
    • Study completion date: Oct 7, 2024 to Jul 7, 2025
    v3
  4. Enrollment target: 100 to 110v2
  5. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
This is a research study designed to test whether a treatment called Intercostal Nerve Cryotherapy is an effective way to help control post-surgical pain for patients undergoing minimally invasive pulmonary resection. There are two treatment groups in this study, a cryotherapy group and control group. Cryotherapy is a method of controlling pain by freezing nerves between the ribs that would transmit pain impulses to the brain.
Trial Details
NCT Number NCT05348447
Lead Sponsor Allegheny Singer Research Institute (also known as Allegheny Health Network Research Institute)
Collaborators: AtriCure, Inc.
Conditions
(from sponsor)		 Cryotherapy Effect, Pain, Postoperative
Related terms Postoperative Pain
Enrollment 110 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov