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

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age2-60
SponsorOman Medical Speciality Board

About this trial

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.

Eligibility criteria

Qualifiers

Patients aged 2 to 60 years.

Patients undergoing EM procedures requiring sedation.

Disqualifiers

Patients with contraindications to any of the sedation agents being studied.

Patients with a history of adverse reactions or allergies to the study medications.

Drug interactions: Patients taking certain medications that may interact adversely with the study medications.

Drug Abuser

Trial design

Treatments tested in this trial

  • atomizer
  • rescue medication
  • Midazolam
  • fentanyl
  • Dexmedetomidine
  • Placabo

Treatment groups

128 Participants
are divided into 2 treatment groups

Sponsors and collaborators