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Not Yet Recruiting NCT07880899

The Impact of Long-term High-risk Drinking on the Effective Dose of Osselidin

Conditions: Sedation

Sex: All
Ages: 18 Years – 64 Years
Healthy volunteers: No
Phase: NA
Enrollment: 110
Sponsor: Affiliated Hospital of Jiaxing University

Location: Affiliated Hospital of Jiaxing University Jiaxing Zhejiang

Summary

this study aims to investigate the effect of chronic high-risk alcohol consumption on the effective dose of oliceridine combined with propofol for painless gastroscopy, so as to provide a reference for rational clinical medication.

Eligibility Criteria

Inclusion Criteria: * This study enrolled patients undergoing elective painless gastroscopy, aged 18-64 years, with American Society of Anesthesiologists (ASA) physical status classification I-II, and body mass index (BMI) of 18-27 kg/m². Exclusion Criteria: * Difficult airway (modified Mallampati grade IV); poorly controlled hypertension (systolic blood pressure ≥160 mmHg and/or diastolic blood pressure ≥100 mmHg); hepatic or renal insufficiency, liver cirrhosis, significant organ dysfunction, severe cardiovascular disease, or arrhythmia; history of long-term use of sedatives, antipsychotics or analgesics; signs of alcohol withdrawal or alcohol addiction (e.g., inability to reduce alcohol intake despite obvious harmful effects, or morning tremors relieved by alcoholic beverages); mental disorders that impede proper self-expression; allergy to study-related medications or acute-phase asthma medications; known or suspected gastrointestinal obstruction; pregnancy or lactation, etc. Exclusion of cases: prolonged examination time due to difficult endoscopic manipulation; severe complications requiring emergency treatment such as hypoxemia and circulatory fluctuation, which violate the study protocol.

Interested in this study? View the official listing for contact and enrollment details.

View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT07880899). StuddyBuddy aggregates publicly available trial information.