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Application and Dosage Study of ciprofol in painless gastrointestinal endoscopy for obese patients

Application and Dosage Study of ciprofol in painless gastrointestinal endoscopy for obese patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600119010
Enrollment
Unknown
Registered
2026-02-13
Start date
2024-03-05
Completion date
Unknown
Last updated
2026-02-16

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

Conditions

Gastroscopy and colonoscopy

Interventions

A Group (Corrected Body Weight):Cycloprofen, induction dose 0.4 mg/kg (calculated by corrected body weight), maintenance dose 1 mg/kg×h (calculated by corrected body weight)
B Group (Total Body Weight):Cycloprofen, induction dose 0.4 mg/kg (calculated by total body weight), maintenance dose 1 mg/kg×h (calculated by total body weight)
C Group (Ideal Body Weight):Cycloprofen, induction dose 0.4 mg/kg (calculated by ideal body weight), maintenance dose 1 mg/kg×h (calculated by ideal body weight)

Sponsors

The Seventh Affiliated Hospital, Sun Yat-sen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 64 Years

Inclusion criteria

Inclusion criteria: 1. It to the indications of painless colonoscopy and can be tolerated; 2. The American Association of Anesthesiologists (ASA) classification as Grade I-II; 3. Age: 18-64 years old; 4. Body mass index (BMI) >= 25 kg/m^2; 5. The patient voluntarily participated and signed the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Allergic to the drugs used in this research; 2. Coronary arteriosclerosis or grade II or above cardiac function; 3. A history of upper respiratory tract infection within 2 weeks; 4. Asthma attack period, uncontrolled hypertension and diabetes, hyperthyroidism or hypothyroidism; 5. Have mental system disorders and cognitive dysfunction; 6. There is a history of abuse of psychotropic drugs and anesthetics. 7. Abnormal liver and kidney functions; 8. Pregnant or lactating women; 9. Age 64 years old; 10. The subjects voluntarily withdrew from the study.

Design outcomes

Primary

MeasureTime frame
Incidence of respiratory depression (SPO2 < 95%);

Secondary

MeasureTime frame
Changes in patient vital signs;Total dose of cycloprofen;Patient satisfaction;

Countries

China

Contacts

Public ContactChi Xinjin

The Seventh Affiliated Hospital, Sun Yat-sen University

chixinjin@yeah.net+86 139 0301 0076

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 19, 2026