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