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Comparison of ciprofol and volatile anesthetics on quality of recovery after abdominal surgery in elderly patients: a randomized controlled study.

Comparison of ciprofol and volatile anesthetics on quality of recovery after abdominal surgery in elderly patients: a randomized controlled study.

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500113342
Enrollment
Unknown
Registered
2025-11-27
Start date
2025-12-01
Completion date
Unknown
Last updated
2025-12-01

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

Conditions

elderly patients undergoing abdominal surgery

Interventions

Ciprofol group:The application of ciprofol throughout anesthesia maintenance
Desflurane group:The application of desflurane throughout anesthesia maintenance
Sevoflurane group:The application of sevoflurane throughout anesthesia maintenance

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age >= 65 years; 2. ASA classification I-III; 3. Scheduled for elective abdominal surgery = 2 hours under general anesthesia and expected to be extubated.

Exclusion criteria

Exclusion criteria: 1. History of myocardial infarction, cardiac failure (NYHA Class III-IV) within 3 months, acute respiratory distress syndrome within 3 months, cerebral infarction within 3 months or severe chronic obstructive pulmonary disease; 2. Known allergies or contraindications to eggs, soy products or study drugs (ciprofol, rocuronium bromide, etc.); 3. With mental illness, long-term use of psychoactive drugs or cognitive dysfunction; 4. History of chronic pain or substance abuse, including alcohol, opioids, or other psychotropic substances; 5. Unable to communicate due to aphasia, severe hearing impairment or other difficulties; 6. Participation in other clinical trials.

Design outcomes

Primary

MeasureTime frame
Quality of recovery;

Secondary

MeasureTime frame
Major surgical complications;Pain scores at rest and during movement;Days Alive at home in the 30 days after Surgery;awakening time;Postoperative Hospital Stay;The incidence of severe nausea and vomiting;The time of first flatus and defecation;Total amount of rescue opioid analgesics;Quality of recovery;The incidence of hyoxemia;Incidence of Delirium;

Countries

China

Contacts

Public ContactXuefei Li

West China Hospital, Sichuan University

lixuefei015@wchscu.cn+86 28 85423593

Outcome results

None listed

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