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A Study on the Safety and Efficacy of Sodium Phosphopentobarbital in Patients with Liver Cirrhosis for Painless Gastrointestinal Endoscopy

A Study on the Safety and Efficacy of Sodium Phosphopentobarbital in Patients with Liver Cirrhosis for Painless Gastrointestinal Endoscopy

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500097793
Enrollment
Unknown
Registered
2025-02-25
Start date
2025-02-25
Completion date
Unknown
Last updated
2025-03-03

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

Conditions

liver cirrhosis

Interventions

Propofol Group:Propofol
Sodium Phosphopentobarbital Group:Sodium Phosphopentobarbital

Sponsors

Renmin Hospital of Wuhan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1.Age between 18 and 60 years old, inclusive, with no gender restrictions; 2.Diagnosed with liver cirrhosis; 3.Presence of symptoms such as hematemesis (vomiting blood), melena (black stool), anemia, or shock; 4.Alanine Aminotransferase (ALT) < 40 U/L, Aspartate Aminotransferase (AST) < 40 U/L; 5.Scheduled for gastrointestinal endoscopy or therapeutic procedures;

Exclusion criteria

Exclusion criteria: 1. Age 60 years; 2.(2) Patients with mean arterial pressure < 65 mmHg; 3.(3) Presence of malignant liver tumors; 4.(4) Presence of severe diseases in other systems, such as cardiovascular and cerebrovascular diseases: a) Cardiovascular system: New York Heart Association (NYHA) Class III or IV heart failure, Adams-Stokes syndrome; a).acute coronary syndrome (ACS) within the past 6 months; b) Patients with psychiatric disorders (such as schizophrenia, depression) and cognitive dysfunction; c) Severe renal insufficiency, patients undergoing dialysis; d) Status epilepticus, convulsions;.traumatic brain injury, intracranial hypertension, cerebral aneurysm; 5 Patients with allergies to sedative or analgesic drugs; 6 Pregnant women.

Design outcomes

Primary

MeasureTime frame
RASS score;

Countries

China

Contacts

Public ContactLu Wang

Renmin Hospital of Wuhan University

wanglu@whu.edu.cn+86 27 88041911

Outcome results

None listed

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