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Effects of Fospropofol Disodium TIVA and IVIH on Surgical Field Quality in Adult ESS

StatusRecruiting
PhaseNot applicable
Started2026-07-12
View on ClinicalTrials.gov ↗
Record status
This record was last updated September 17, 2026 (before its estimated September 30, 2026 completion). Its status may not reflect the trial's current state.

Amendment history

2026-09-18
notable
Recruitment opened
Primary completion moved earlier: 2026-12-31 → 2026-09-30
Completion moved earlier: 2027-01-31 → 2026-12-31
197 trials monitored
See 2 trials at risk
Endoscopic sinus surgery (ESS) is a primary surgical approach for treating chronic rhinosinusitis, nasal polyps, and other conditions that are unresponsive to conservative therapy. A clear surgical field is a critical prerequisite for ensuring precision, efficiency, and the avoidance of injury to vital structures such as the orbit and the skull base. Currently, the anesthetic regimens commonly used for ESS include total intravenous anesthesia (TIVA), inhalational anesthesia (IA), and intravenous-inhalational combined anesthesia (IVIH). However, there remains controversy regarding the comparative effects of these three modalities on surgical field quality. IVIH, as an anesthetic strategy that integrates the advantages of both intravenous and inhalational agents, is widely employed in clinical practice. In the context of ESS, it may reduce the dose of individual agents through combination therapy, thereby minimizing dose-related adverse effects. Some studies have shown that propofol-based TIVA provides better surgical field conditions than inhalational anesthetics (e.g., desflurane, sevoflurane), but does not significantly reduce total blood loss or shorten operative time. Nevertheless, propofol is associated with drawbacks such as injection pain and propofol infusion syndrome. Fospropofol disodium, a water-soluble prodrug of propofol, offers a significant advantage in reducing injection pain and provides more stable hemodynamic profiles.
Trial Details
NCT Number NCT07788157
Lead Sponsor Tongji Hospital
Conditions Fospropofol Disodium
Enrollment 144 participants
Start Date 2026-07-12
Primary Completion 2026-09-30 (estimated)
Study Completion 2026-12-31 (estimated)
Updated on ClinicalTrials.gov 2026-09-17