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The Impact of Low-Dose Esketamine Combined With Ciprofol on the Quality of Early Postoperative Recovery Among Elderly Patients Undergoing Painless Gastroscopy

StatusActive, Not Recruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗
Record status
This record was last updated May 7, 2025 (before its estimated July 15, 2025 completion). Its status may not reflect the trial's current state.

Record History

  1. Lead sponsor: Subei People's Hospital of Jiangsu Province to Northern Jiangsu People's Hospital
    • Trial status: Not Yet Recruiting to Active, Not Recruiting
    • Primary and study completion dates: May 2025 to Jul 15, 2025
    • Start date changed from estimate of Oct 2024 to Oct 10, 2024
    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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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.
To explore the impact of esketamine combined with ciprofol on the quality of early postoperative recovery in elderly patients undergoing painless gastroscopy, as well as the effectiveness and safety of this regimen.
Trial Details
NCT Number NCT06617039
Lead Sponsor Northern Jiangsu People's Hospital
Conditions
(from sponsor)		 Quality of Postoperative Recovery
Enrollment 376 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov