Clinical Trials Directory

Trials / Completed

CompletedNCT05911776

Nasal Packing Versus Intravenous Dexmedetomidine in Turbinate Surgeries

Nasal Packing Versus Intravenous Dexmedetomidine in Turbinate Surgeries: A Randomized Double-Blinded Trial

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
60 (actual)
Sponsor
Kafrelsheikh University · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

Comparing of nasal packing DEX and IV DEX for controlling the intraoperative bleeding after turbinate surgery.

Detailed description

Dexmedetomidine (DEX) is a highly selective α2 adreno-receptor agonist with higher affinity to a2 adreno-receptor than clonidine, and this makes DEX primarily sedative and anxiolytic. The elimination half-life of DEX (t1/2b) is 2 h and the redistribution half-life (t1/2a) is 6 min, and this short half-life makes it an ideal drug for intravenous titration. Potentially desirable effects include decreased requirements for other anesthetics and analgesics.

Conditions

Interventions

TypeNameDescription
DRUGNasal packing Dexmedetomidinepatients will receive nasal packing Dexmedetomidine (1.5 μg/kg intranasal dexmedetomidine diluted with saline) and Intravenous infusion saline.
DRUGIntravenous Dexmedetomidinepatients will receive 0.5 μg/kg bolus over 10 min then 0.1- 0.4 μg/kg Intravenous infusion Dexmedetomidine and nasal packing with saline.

Timeline

Start date
2023-06-30
Primary completion
2024-02-27
Completion
2024-02-27
First posted
2023-06-22
Last updated
2024-03-12

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT05911776. Inclusion in this directory is not an endorsement.