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Early Outcomes of Spontaneous vs. Negative-pressure Drainage After Coronary Artery Bypass Grafting

StatusActive, Not Recruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗
Trial flagged as At Risk
Primary endpoint reworded 3 of 3 changed
See other at-risk trials from Başakşehir Çam & Sakura City Hospital

Record History

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  1. Primary endpoint(s) modified Show 4 more changesShow less
    • Eligibility criteria expanded, about 39 words
    • Secondary endpoints revised (2)
    • Study description shortened, about 93 words
    • Study title shortened, about 11 words
  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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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 purpose of this prospective, randomized controlled clinical trial is to evaluate early postoperative outcomes and fluid drainage dynamics between continuous active negative-pressure chest drainage (-10 mmHg) and standard spontaneous closed underwater-seal drainage in adult patients undergoing elective isolated coronary artery bypass grafting (CABG).
Trial Details
NCT Number NCT07814573
Lead Sponsor Başakşehir Çam & Sakura City Hospital
Conditions
(from sponsor)		 Drainage, Complications Due to Coronary Artery Bypass Graft, Coronary Artery Bypass Graft (CABG)
Enrollment 400 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov