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Comparison Between Two Drugs in Sedation of Upper GI Endoscopy

Sponsored by Zagazig University

NCT ID
NCT07423676
Target Enrollment
52 participants
Start Date
2026-03-01
Est. Completion
2026-05-02

About This Study

The goal of this clinical trial is to compare time of sedation between two drugs administered to patients undergoing upper gastrointestinal endoscopy Primary outcome : Time of sedation : is the time to reach sedation score of 5 according to modified Ramsay sedation score starting from the time of injecting bolts dose of study drugs Secondary outcome : * Recovery time :is the time to reach score 2 of modified Ramsay sedation score starting from injecting bolus dose of study drugs . * Hemodynamics (MAP,HR) \& oxygen saturation * Drug side effects (nausea,vomitting,agitation) * Endoscopist satisfaction

Conditions Studied

Sedation During GI Endoscopy

Eligibility

Age:21 Years - 60 Years
View full eligibility criteria
Inclusion Criteria

* Patient acceptance
* Adults aged 21-60 years.
* Both sexes
* BMI\<35 kg/m2
* ASA physical status :I\& II
* Patients Undergoing Gastrointestinal endoscopy
* Duration \<30mintues

Exclusion Criteria:

* • Known allergy to any of the study drugs

  * Unstable Cardiovascular disease
  * Moderate to severe respiratory diseases

Interested in this trial?

Contact the study team to learn more about eligibility and enrollment.

Ahmed Esam Hamad, Register
CONTACT
+201095529439tahawy188@gmail.com
View on ClinicalTrials.gov
Data Source
ClinicalTrials.gov

Last updated from source