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A randomized clinical study of the impact of preoperative precision evaluation and intervention on prognosis and regression in elderly patients undergoing painless gastrointestinal endoscopy

A randomized clinical study of the impact of preoperative precision evaluation and intervention on prognosis and regression in elderly patients undergoing painless gastrointestinal endoscopy

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300067729
Enrollment
Unknown
Registered
2023-01-19
Start date
2023-01-20
Completion date
Unknown
Last updated
2023-05-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Gastrointestinal Diseases

Interventions

Experimental:Supplementation of glucose, electrolytes, and balanced fluids based on precise assessment

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age greater than 65 years; 2. Inpatients undergoing elective painless gastroenteroscopy; 3. ASA classification I-III.

Exclusion criteria

Exclusion criteria: 1. Surgical time longer than 2 hours; 2. Poor compliance and inability to cooperate with follow-up visits; 3. Refusal to sign an informed consent form; 4. Combined history of angina pectoris and myocardial infarction,heart failure; 5. History of arrhythmia (including atrial fibrillation, atrial flutter, atrioventricular block, frequent premature atrial contractions and prematureventricular contractions); 6. Use of diuretics; 7. Patients with combined inflammatory bowel disease; 8. Combined inferior vena cava disease (including Buga syndrome,congenital developmental anomaliesinferior vena cava obstruction); 9. Patients who fast for more than 2 days due to their condition; 10. Patients with allergy to anesthetic drugse.

Design outcomes

Primary

MeasureTime frame
Perioperative anesthesia and surgery-related adverse events;Gastrointestinal adverse events: bleeding, perforation;

Secondary

MeasureTime frame
Postoperative subjective discomfort: symptoms of thirst, hunger, nausea and vomiting, drowsiness, fatigue, dizziness;Postoperative awakening time;PACU length of stay;quality ofpostoperative recovery scores;Patient satisfaction;Length of stay;Hospitalization expensese;

Countries

China

Contacts

Public ContactRurong Wang

West China Hospital, Sichuan University

wangrurong@scu.edu.cn+86 18980601563

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026