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Trials / Not Yet Recruiting

Not Yet RecruitingNCT07166666

Study Comparing Atomizerd Midazolam & Fentanyl and Dexmedomidine for Procedural Sedation in Adult and Pediatric Patient (2 to 60 Years Old)

Status
Not Yet Recruiting
Phase
N/A
Study type
Interventional
Enrollment
128 (estimated)
Sponsor
Oman Medical Speciality Board · Other Government
Sex
All
Age
2 Years – 60 Years
Healthy volunteers
Not accepted

Summary

To evaluate the depth of sedation, as well as onset, and recovery times, satisfaction of sedation , adverse events associated with Atomized Midazolam \& Fentanyl and Dexmedetomidine during procedural sedation in a diverse population spanning from 2 to 60 years old at these three prominent Omani healthcare facilities.

Conditions

Interventions

TypeNameDescription
DEVICEatomizeruse atomizer to provide the medication in procedure sedation
DRUGrescue medicationwill be used as rescue if the atomizer medication not fully sedated
DRUGMidazolamIntranasal administration for procedural sedation.
DRUGfentanylIntranasal administration for procedural sedation.
DRUGDexmedetomidineIntranasal administration for procedural sedation.
DRUGPlacabouse atomizer to provide the placebo in procedure sedation

Timeline

Start date
2025-09-01
Primary completion
2026-09-30
Completion
2026-10-01
First posted
2025-09-10
Last updated
2025-09-10

Locations

1 site across 1 country: Oman

Source: ClinicalTrials.gov record NCT07166666. Inclusion in this directory is not an endorsement.