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Neurologic Safety of remimazolam for cirrhotic patients undergoing EVL and/or EVS

The neurological safety of different sedative drugs used for cirrhotic patients undergoing EVL and/or EVS

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200066161
Enrollment
Unknown
Registered
2022-11-25
Start date
2022-11-28
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

minimal hepatic encephalopathy

Interventions

Propofol group:propofol drug
remimazolam group:remimazolam drug
sevoflurane group:sevoflurane drug

Sponsors

Liaocheng People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: patients undergoing esophagogastric varices and / or sclerotherapy in the center of digestive endoscopy in our hospital. Patients should have a complete medical history, physical examination, chest X-ray, and electrocardiogram examination, as well as complete blood routine, liver and kidney function, and virus screening and abdominal ultrasound examination. Patients aged 18 to 80 years; patients with cirrhosis with endoscopic descending EVL and / or EVS; esophageal varicose pattern grade G ~G; liver function Child-Pugh class A, B, or C; patients who agreed to receive endoscopic treatment and signed informed consent.

Exclusion criteria

Exclusion criteria: The American Association of Anesthesiologists (American Society of Anesthesiologists, ASA) grades IV or V; alcohol, opioid, or sedative-hypnotic addiction; clinically detectable hepatic encephalopathy, psychiatric, psychiatric, or active neurological disorders; neurological diseases such as Alzheimer's or Parkinson's; perioperative hemorrhagic shock; known allergy to egg products, tofu, soy, propofol, or benzodiazepines.

Design outcomes

Primary

MeasureTime frame
NCT-A DST;

Secondary

MeasureTime frame
Quality of Recovery-40 Questionnaire,Qo R-40;spontaneous breathing time;awaking time;extubation time;Steward MOAA/S;Postoperative adverse effects;Pittsburgh Sleep Quality Index (PSQI);health-related quality of life (HRQoL);

Countries

CHINA

Contacts

Public ContactFu Shi

Liaocheng People's Hospital

317449197@qq.com+86 18006353835

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Sep 6, 2026