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Ciprofol in the induction of general anesthesia and the quality of recovery in elderly patients with gastrointestinal tumors

Ciprofol in the induction of general anesthesia and the quality of recovery in elderly patients with gastrointestinal tumors

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100044196
Enrollment
Unknown
Registered
2021-03-12
Start date
2021-04-01
Completion date
Unknown
Last updated
2021-08-30

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

Conditions

Gastrointestinal tumors

Interventions

Sponsors

Suzhou Municipal Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Aged 65-85 years, no gender limit; (2) American Anesthesiologists (ASA) Grade I-II; (3) Elderly patients with gastrointestinal tumors undergoing elective surgery; (4) Body mass index (BMI) >= 18 and <= 30kg/m2; (5) The vital signs are relatively stable; (6) Able to understand the research process and methods, and voluntarily participate in this research.

Exclusion criteria

Exclusion criteria: (1) Those who have general anesthesia contraindications or have a history of anesthesia accidents in the past; (2) Those who are known or suspected to be allergic or contraindicated to propofol injection, cyclopofol injection excipients, benzodiazepines, opioids, muscle relaxants, etc.; (3) Patients with acute upper respiratory tract infection, asthma attack or acute severe throat disease; (4) Complicated with history of brain loss, intracranial hypertension, stroke, cerebrovascular accident, etc.; (5) Respiratory insufficiency, obstructive pulmonary disease, difficult airway, or difficulty in tracheal intubation (modified Markov score is III or IV); (6) Uncontrolled hypertension, hypotension and diabetes; (7) Severe arrhythmia, heart failure, unstable angina, myocardial infarction, etc.; (8) Severe liver dysfunction or severe renal insufficiency; (9) History of alcoholism or drug dependence; (10) Abuse or long-term use of narcotic, sedative, and analgesic drugs; (11) Those who have a history of mental illness; (12) Those who have participated in any drug clinical trial within 1 month before screening; (13) The investigator believes that there are any other subjects who are not suitable to participate in this trial.

Design outcomes

Primary

MeasureTime frame
Success rate of general anesthesia induction;recovery time;

Countries

China

Contacts

Public ContactLi Hua

Suzhou Municipal Hospital

15962229836@163.com+86 15962229836

Outcome results

None listed

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