Effect of Different General Anesthesia Protocol on Postoperative Recovery and Sleep Quality in Patients undergoing Ambulatory Surgery

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR2200063987

Enrollment

Unknown

Registered

2022-09-22

Start date

2022-09-23

Completion date

Unknown

Last updated

2023-04-17

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

Conditions

None listed

Interventions

Group S:Anesthesia maintainess: sevoflurane

Group D:Anesthesia maintainess: desflurane

Group P:Anesthesia maintainess: propofol

Eligibility

Sex/Gender

All

Age

18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Aged >= 18 years; 2. ASA class I-III; 3. Scheduled to undergo ambulatory surgery under general anesthesia; 4. Signed informed consent.

Exclusion criteria

Exclusion criteria: 1. Cannot cooperate with the study or refuse to participate in the study for any reason; 2. Known allergy to any anesthetic drug used in the study; 3. Patients with liver dysfunction, renal dysfunction, heart disease, thyroid dysfunction and endocrine disease; 4. Patients with neurological diseases or mental diseases; 5. Patients with morbid obesity, obstructive sleep apnea hypopnea syndrome; 6. Alcoholics or drug abuse; 7. Patients transferred to intensive care unit after operation; 8. Participate in other clinical trials within 30 days before enrollment.

Design outcomes

Primary

Measure	Time frame
15-item Recovery Quality Scoring Scale (QoR-15);	—

Secondary

Measure	Time frame
Pittsburgh Sleep Quality Index ;numeric rating scale score for pain;extubation time;incidence of emergence agitation;length of PACU stay;incidence of postoperative nausea and vomiting;length of sleep;modified Aldrete score;	—

Countries

China

Contacts

Public ContactWang Siyang

Zhongshan Hospital, Fudan University

wangsiyang2010@foxmail.com+86 15221318131

Outcome results