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Clinical study of ciprofol in digestive endoscopy

Clinical study of ciprofol in digestive endoscopy

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200061727
Enrollment
Unknown
Registered
2022-07-01
Start date
2022-07-10
Completion date
Unknown
Last updated
2023-04-03

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

Conditions

painless digestive endoscopy

Interventions

group A:ciprofol+alfentanil 7µg/kg
group B:propofol+alfentanil 7µg/kg
group C:1.3 times the median effective dose of ciprofol + alfentanil 7µg/kg
group D:1.3 times the median effective dose of propofol + alfentanil 7µg/kg

Sponsors

The Second Affiliated Hospital of Hainan Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 64 Years

Inclusion criteria

Inclusion criteria: 1. Patients who voluntarily undergo painless gastrointestinal endoscopy from July 10; 2. 2022 to December 31; 3. 2023, regardless of gender; 4. age 18 to 64 years old' 5. BMI 18 to 28 kg/?; 6. ASA I or II; 7. sign an informed consent form for anesthesia.

Exclusion criteria

Exclusion criteria: 1. Patients with contraindications to routine gastrointestinal endoscopy, contraindications to anesthesia; 2. esophageal cancer, and a history of taking medications that affect the results of the test, pregnant and lactating women; 3. those who require endotracheal; 4. Those with underlying esophageal pathology.

Design outcomes

Primary

MeasureTime frame
mean arterial pressure;oxygen saturation;wake up of time;time of departure from the hospital;

Secondary

MeasureTime frame
incidence of injection pain;incidence of nausea and vomiting;incidence of resuscitation agitation;

Countries

China

Contacts

Public ContactHu Sun

the Second Affiliated Hospital of Hainan Medical University

sunhu09@163.com+86 13617518996

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 9, 2026