Clinical Trial

Proactive Temperature Management in CRS-HIPEC for Prevention of Delirium

Not Yet Recruiting
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Record status
This record was last updated January 30, 2026 (before its estimated March 20, 2026 completion). Its status may not reflect the trial's current state.
Summary
This randomized controlled trial evaluates the efficacy of a proactive Goal-Directed Temperature Management (GDTM) protocol in reducing postoperative delirium among patients undergoing Cytoreductive Surgery (CRS) with Hyperthermic Intraperitoneal Chemotherapy (HIPEC) for pseudomyxoma peritonei. CRS-HIPEC presents a unique physiological challenge characterized by a biphasic thermal trajectory: potential hypothermia during extensive surgery followed by rapid iatrogenic hyperthermia during perfusion. This study compares a standardized GDTM strategy-which incorporates strict normothermia maintenance and anticipatory pre-cooling prior to perfusion-against standard reactive thermal management. The primary objective is to determine if optimized thermoregulation can attenuate thermal variability and improve early neurocognitive recovery.
Trial Details
NCT Number NCT07378371
Lead Sponsor Aerospace Center Hospital
Conditions Pseudomyxoma Peritonei, Postoperative Delirium (POD)
Enrollment 174 participants
Start Date 2026-02-01
Primary Completion 2026-03-20 (estimated)
Study Completion 2026-05-01 (estimated)
Updated on ClinicalTrials.gov 2026-01-30