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Comparison of anesthesia effect between cyclopofol injection and propofol injection in painless colonoscopy: a prospective randomized controlled study

Comparison of anesthesia effect between cyclopofol injection and propofol injection in painless colonoscopy: a prospective randomized controlled study

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100053226
Enrollment
Unknown
Registered
2021-11-16
Start date
2021-11-14
Completion date
Unknown
Last updated
2022-09-20

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

Conditions

Gastrointestinal dysfunction

Interventions

control group:Induction with 2.0 mg / kg propofol
experimental group:Induction with 0.4mg / kg ciprofol

Sponsors

Liaoning Provincial People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Patients who need colonoscopy for gastrointestinal diseases; 2. Aged 18-70 years, no gender limit, ASA I-II grade; 3. Obtain the informed consent of the patient or his guardian.

Exclusion criteria

Exclusion criteria: 1. BMI > 30kg/m^2; 2. History of allergy to propofol, soy, egg or opioids; 3. Known or predicted airway difficulty (such as Mallampati grade 3 or 4); 4. Severe hypertension (the control of hypertension is still above grade III after taking medicine), cardiac insufficiency (LVEF: 1.5 times the upper limit of normal or GFR < 40ml/min); 7. History of taking sedatives, antidepressants, alcoholism and drug addiction; 8. Patients who are unable to understand the research protocol, difficult to communicate in language, and uncooperative; 9. Pregnant and lactating patients.

Design outcomes

Primary

MeasureTime frame
Diagnosis and treatment operation;Gender;Age;Height;Weight;Body mass index;ASA classification;Systolic pressure;Diastolic pressure;Mean arterial pressure;Heart rate;Oxygen saturation;Dosage of ciprofol/propofol;Additional ciprofol / propofol dose;Administration time;Lowest oxygen saturation;Lowest heart rate;Lowest mean arterial pressure;Onset time;Operation time;Recovery time;Room departure time;Injection pain;Choking cough;Muscle fasciculation;Hypoxemia;Apnea;Airway obstruction;Hypotension;Tachycardia;Bradycardia;Nausea;Vomit;Drowsiness;Vertigo;Postoperative pain score;Patient satisfaction;Surgeon satisfaction;Intraoperative awareness;

Countries

China

Contacts

Public ContactGao Shihui

Liaoning Provincial People's Hospital

835606336@qq.com+86 17824910568

Outcome results

None listed

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