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Intercostal Nerve Block for Pain Management After Uniportal Video-assisted Thoracoscopic Surgeries

Study acronym: VATS
StatusNot Yet Recruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗
Record status
This record was last updated April 1, 2025 (before its estimated May 5, 2026 completion). Its status may not reflect the trial's current state.

Record History

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  1. Study description revised
    • Site contacts updated at 2 of 2 sites
    v2
  2. 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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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.
The goal of this clinical trial is to compare the safety and effectiveness of the three intercostal nerve blocks used in pain management in uniportal (one port) thoracoscopic surgeries: internal intercostal nerve blocks (ICNB), external ICNB, and Intercostal catheters. Participants will be randomly assigned to three groups: * First group will undergo internal intercostal nerve block * Second group will be given external intercostal nerve block * Third group will have an intercostal catheter Researchers will compare the three groups to see their impact on post-operative pain management in uniportal VATS.
Trial Details
NCT Number NCT06838026
Lead Sponsor Al-Quds University
Collaborators: Al-Ahli Hospital, Hebron, Saint Joseph Hospital, East Jerusalem
Conditions
(from sponsor)		 Thoracic, Pain, Postoperative, Analgesia, Satisfaction, Patient
Related terms Agnosia, Patient Satisfaction, Postoperative Pain
Enrollment 90 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov