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Comparison of the efficacy and safety of oral or transanal double balloon enteroscopy under general anaesthesia maintained by ciprofol versus propofol

Comparison of ciprofol versus propofol for the induction of general anesthesia during double balloon enteroscopy: A randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500096681
Enrollment
Unknown
Registered
2025-02-04
Start date
2024-01-06
Completion date
Unknown
Last updated
2025-02-10

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

Conditions

Small Intestine Related Diseases

Interventions

ciprofol group:ciprofol 0.2mg/kg
Propofol group:Propofol 1.5mg/kg

Sponsors

900th Hospital of the United Logistics Force
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. patients who meet the indications for small boweloscopy; 2. Age >=18 and <=80 years; 3. American Society of Anaesthesiologists grade I to III; 4. Willing to sign the informed consent and strictly comply with the study protocol.

Exclusion criteria

Exclusion criteria: 1.Allergy to propofol, cypropofol, fentanyl and its antidotes, eggs or soya; 2.Combined major organ dysfunction, various acute conditions, systemic infectious diseases; 3.Combination of severe cardio-cerebral and pulmonary diseases; 4.Combined with mental diseases and cognitive disorders; 5.Presence of contraindications to anaesthesia and surgery; 6.Long-term use of sedative drugs; 7.Pregnant and lactating women; 8.Participation in any pharmacological clinical trials within the last 3 months; 9.Subjects who, in the opinion of the investigator, have any other factors that make participation in this clinical study inappropriate.

Design outcomes

Primary

MeasureTime frame
Success rate of enteroscope;

Secondary

MeasureTime frame
Induction time;Insertion time;Examination time;Awakening time;Orientation recovery time;Time out of the post-anaesthetic care unit;blood pressure;heart rate ;respiratory rate ;saturation of peripheral oxygen ;modified observer's assessment of alertness or sedation;Intraoperative adverse events;postoperative adverse reaction;Satisfaction Assessment;

Countries

China

Contacts

Public ContactHe Xiaojian

Department of Gastroenterology, 900th Hospital of the United Logistics Force

627858017@qq.com+86 177 5892 9990

Outcome results

None listed

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