Clinical Trials Directory

Trials / Recruiting

RecruitingNCT06756594

Efficacy of Dexmedetomidine-Propofol Versus Ketamine-Propofol for Sedation

Efficacy of Dexmedetomidine-Propofol Versus Ketamine-Propofol for Sedation During Gastrointestinal Endoscopy

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
100 (estimated)
Sponsor
Sohag University · Academic / Other
Sex
All
Age
18 Years – 60 Years
Healthy volunteers
Not accepted

Summary

This study aims to compare efficacy of sedation between Dexmedetomidine-Propofol and Ketamine-Propofol combinations in the upper or lower gastrointestinal system endoscopy. We compare between 2 combinations as regard hemodynamic stability, post operative side effects as occurrence of delirium, nausea, vomiting, headache, hallucination or agitation.

Conditions

Interventions

TypeNameDescription
DRUGDexmedetomidine-Propofolefficacy of sedation with Dexmedetomidine-Propofol combination in the upper or lower gastrointestinal system endoscopy.
DRUGKetamine-Propofolefficacy of sedation with Ketamine-Propofol combination in the upper or lower gastrointestinal system endoscopy.

Timeline

Start date
2024-11-12
Primary completion
2025-06-11
Completion
2025-06-11
First posted
2025-01-03
Last updated
2025-01-03

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT06756594. Inclusion in this directory is not an endorsement.

Efficacy of Dexmedetomidine-Propofol Versus Ketamine-Propofol for Sedation (NCT06756594) · Clinical Trials Directory