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Randomized controlled trial for endoscopy with propofol versus ciprofol on psychometric tests and critical flicker frequency in people with cirrhosis

Endoscopy with propofol versus ciprofol on psychometric tests and critical flicker frequency in people with cirrhosis

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100051042
Enrollment
Unknown
Registered
2021-09-10
Start date
2021-10-01
Completion date
Unknown
Last updated
2022-05-16

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

Conditions

cirrhosis

Interventions

Control group:propofol

Sponsors

Zigong Fourth People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
19 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Patients between the ages of 19 and 75 years for the evaluation of portal hypertension; 2. ASA I-III; 3. Child-Turcotte-Pugh A, B; 4. Body mass index (BMI) >= 18 and = 10 and = 95% when breathing air; systolic (SBP) >= 90mmHg and = 60mmHg and = 55 and <= 100 beats/min; 6. Be able to understand the research process and methods, and voluntarily participate in this research.

Exclusion criteria

Exclusion criteria: 1. Patients with American Society of Anesthesiology (ASA) class IV or V physical condition; 2. Active gastrointestinal bleeding; 3. Continued drinking; 4. mental illness; 5. Drug abuse; 6. Patients taking neuroactive drugs (such as benzodiazepines, antiepileptic drugs, and any other sedatives and anesthetics); 7. Patients with clinical symptoms of hepatic encephalopathy; 8. Patients with visual or mental disorders who cannot complete the HE examination; 9. Those with contraindications to general anesthesia or those who have had a history of anesthesia accident in the past; 10. Known or suspected allergic or contraindicated to propofol injection, cyclopofol injection excipients, opioids, etc.; 11. Combined with craniocerebral loss, intracranial hypertension, stroke, unstable angina, myocardial infarction; 12. Those who have participated in any drug clinical trials within 1 month before screening; 13. Pregnant and lactating women; fertile women or men who are unwilling to use contraception throughout the trial period; subjects (including male subjects) who have a pregnancy plan within 1 month after the trial; 14. Subjects who are considered by the investigator to have any other factors that are not suitable for participating in this trial.

Design outcomes

Primary

MeasureTime frame
psychometric tests;

Secondary

MeasureTime frame
Cognitive function score;Stroop tests;critical flicker frequency;satisfaction survey;Hemodynamic parameters;The success rate of endoscopy diagnosis and treatment;side effect;

Countries

China

Contacts

Public ContactChen Guanyu

Zigong Fourth People's Hospital

741755319@qq.com+86 13696221073

Outcome results

None listed

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