RecruitingNot Applicable

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

China226 participantsStarted 2024-01-01

Plain-language summary

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.

Who can participate

Age range65 Years – 100 Years

SexALL

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Inclusion criteria

✓. Age greater than 65 years old, regardless of gender
✓. ASA is classified as Class II and III;
✓. BMI 18-28 kg/m2;
✓. Patients undergoing examination or treatment outside the operating room;
✓. FRAIL scale score ≥ 3 points 6 The patient voluntarily participated in this study and signed an informed consent form.

What they're measuring

Adverse cardiovascular events

Timeframe: during the examination and recovery room time(up to 2 hours)

Trial details

NCT IDNCT06192082

SponsorBeijing Friendship Hospital

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2026-02-12

Contact for this trial

Haijun Hou, MD

+8618612568228 77790690@qq.com

View on ClinicalTrials.gov More Anesthesia trials