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Adverse Cardiovascular Events During Painless Gastroscopy Diagnosis and Treatment in Elderly Frail Patients

Study acronym: frail
StatusRecruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗

Record History

  1. Enrollment target: 108 to 226
    • Primary and study completion dates: Feb 12, 2024 to Feb 12, 2026
    • Trial status: Completed to Recruiting
    • Site details revised
    v3
  2. Trial status: Not Yet Recruiting to Completedv2 Show 4 more changesShow less
    • Enrollment target: estimated 226 to confirmed 108
    • Study sites: 0 to 1
    • Primary completion date changed from estimate of Mar 30, 2024 to Feb 12, 2024
    • Study completion date changed from estimate of Apr 30, 2024 to Feb 12, 2024
  3. 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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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.
This study aims to compare the effects of conscious sedation and intravenous general anesthesia on cardiovascular events in frail patients undergoing digestive endoscopy diagnosis and treatment.
Trial Details
NCT Number NCT06192082
Lead Sponsor Beijing Friendship Hospital
Conditions
(from sponsor)		 Anesthesia
Enrollment 226 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov