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The effect of geriatric nutritional risk index (GNRI) on the quality of recovery in patients undergoing general anesthesia

The effect of geriatric nutritional risk index (GNRI) on the quality of recovery in patients undergoing general anesthesia: an observational study

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200067171
Enrollment
Unknown
Registered
2022-12-28
Start date
2023-01-01
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

Cough

Interventions

high geriatric nutritional risk index (GNRI) group:N/A
low geriatric nutritional risk index (GNRI) group:N/A

Sponsors

The First Affiliated Hospital of Sun Yat-sen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to 99 Years

Inclusion criteria

Inclusion criteria: (i) age =65 years; (ii) The American Society of Anesthesiologists (ASA) Physical Status Classification I, II and III; (iii) scheduled to undergo elective surgery under general anaesthesia requiring tracheal intubation; (iv)patients can tolerate operation and are no allergic reaction to anesthetics; and (v) signed informed consent.

Exclusion criteria

Exclusion criteria: (i) patients underwent neurosurgery surgery, cardiovascular surgery or nighttime surgery; (ii) combination of other vital organ dysfunctions: including severe liver and kidney dysfunction; organic brain diseases, specifically aneurysmal vascular disease or arteriovenous malformation and cerebral hemorrhage; severe hypertension, coronary heart disease, cardiac insufficiency (NYHA >= grade III); abnormal coagulation function; severe respiratory system diseases; (iii) patients with preoperative behavior disorder or combined mental illness who have used psychotropic drugs; (iv) patients with the long-term use of sedative drugs or glucocorticoid; (v) those with a history of alcohol or drug dependence; and (vi)patients deemed unsuitable for inclusion by other investigators.

Design outcomes

Primary

MeasureTime frame
cough before extubation;

Secondary

MeasureTime frame
time from the end of surgery to spontaneous breathing recovery;time from the end of surgery to eye opening;time from cessation of sedation administration to extubation;time from the end of surgery to orientation recovery;PACU length-of-stay;

Countries

China

Contacts

Public ContactZhu Qiongfang

The First Affiliated Hospital of Sun Yat-sen University

ZhuQiong_Fang@126.com13533598801

Outcome results

None listed

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