Skip to content

Predictive value of preoperative frailty assessment for quality of recovery from anesthesia in elderly patients undergoing painless gastrointestinal endoscopy: a prospective cohort study

Predictive value of preoperative frailty assessment for quality of recovery from anesthesia in elderly patients undergoing painless gastrointestinal endoscopy: a prospective cohort study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000029715
Enrollment
Unknown
Registered
2020-02-09
Start date
2020-02-10
Completion date
Unknown
Last updated
2020-02-10

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

Conditions

Frailty

Interventions

Cohort 2:No Frailty

Sponsors

The First Affiliated Hospital of College of Medicine of Zhejiang University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Aged 65 years or above; 2. ASA class I-III; 3. Inpatients who planned to have an elective gastrointestinal endoscopy under general anesthesia.

Exclusion criteria

Exclusion criteria: 1. Patients with contraindications for routine endoscopic procedures or patients who refuse anesthesia; 2. Patients who require endotracheal intubation; 3. Anesthesia is administered for less than 30 minutes or more than 90 minutes; 4. Patients with uncontrolled, potentially life-threatening circulatory and(or) respiratory diseases; and(or) severe liver dysfunction (Child-Pugh C), and(or) severe renal dysfunction, and(or) acute upper gastrointestinal hemorrhage with shock, and(or) severe anemia, and(or) gastrointestinal obstruction with gastric content retention; 5. Patients without escort or guardian; 6. Allergic to narcotic drugs, opioids or other anesthesia-related drugs; 7. Patients with difficult airway; 8. Patients with severe neurological or psychiatric disorders; 9. Substance abuser; 10. Patients with morbid obesity; 11. Patients with high risk of anesthesia; 12. The disabled.

Design outcomes

Primary

MeasureTime frame
Modified Aldrete Score;Modified Post Anesthetic Discharge Scoring System scale;Sensitivity;Specificity;False positive rate;False negative rate;Accuracy;

Secondary

MeasureTime frame
Awakening time;Numerical Rating Scale;Complications;Dosage of propofol;Vital signs;

Countries

China

Contacts

Public ContactFang Xiangming

Department of Anesthesiology, The First Affiliated Hospital of College of Medicine of Zhejiang University

xiangming_fang@163.com+86 13857161019

Outcome results

None listed

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