Join us at Health Research Day — June 6th at Canton Waterfront Park, Baltimore!   Learn More →
← Back to all trials
Completed NCT07190612

Efficacy of Propofol Combination With Either Ketamine, Dexmedetomidine or Midazolam for Sedation During Upper Gastrointestinal Endoscopic Procedures

Conditions: Upper Gastrointestinal Endoscopy, Anesthesia

Sex: All
Ages: 18 Years – 65 Years
Healthy volunteers: No
Phase: PHASE4
Enrollment: 75
Sponsor: Ain Shams University

Location: Faculty of Medicine Cairo

Summary

The investigators are comparing the efficacy of three different sedative agents in gastrointestinal endoscopic procedures.

Eligibility Criteria

Inclusion Criteria: * Both male and female patients aged between 18 and 65 years * Patients who are scheduled for elective upper gastrointestinal endoscopic procedures with sedation * Patients who are classified as ASA (American Society of Anesthesiologists) I and II Exclusion Criteria: * Patient's refusal to participate * Respiratory compromise as patients with respiratory failure or with active chest conditions, e.g., bronchial asthma or pneumonia * Cardiovascular compromise including heart failure and shocked patients * Severe uncontrolled hematemesis with shock or risk of aspiration. * Patients who are allergic or have any contraindications to any of the used drugs. * Patients who have a chronic neuropsychiatric disorder or are on a neuropsychiatric drug. * Patients on long-term sedative medication have a history of drug or alcohol abuse. * Pregnancy and lactation

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

View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT07190612). StuddyBuddy aggregates publicly available trial information.