Clinical Trials Directory

Trials / Completed

CompletedNCT05781035

Dexmedetomidine Versus General Anesthesia on the Diagnosis of Endobronchial US-Guided Transbronchial Needle Aspiration

Moderate Sedation by Dexmedetomidine Versus General Anesthesia on the Diagnostic Yield of Endobronchial Ultrasound-Guided Transbronchial Needle Aspiration: A Randomized Controlled Study

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

Summary

The aim of this study is to compare dexmedetomidine as moderate sedation versus general anathesia on the diagnostic yield of Endobronchial Ultrasound-Guided Transbronchial Needle Aspiration

Detailed description

Endobronchial ultrasound (EBUS)-guided transbronchial needle aspiration (EBUS-TBNA) has emerged as a highly effective, minimally invasive technique for sampling peribronchial, mediastinal, and lung masses for pathologic examination with low rate of complications, and costs. Dexmedetomidine, is a high-affinity adrenergic agonist of the alpha 2 receptor, is a potential alternative sedative. The use of dexmedetomidine does not lead to respiratory depression, or to a decline in cognitive skills or patient cooperation. This is because dexmedetomidine acts on the alpha-2 receptors in the locus coeruleus, in contrast to other sedatives (midazolam and propofol) which act on GABA receptors/cerebral cortex.

Conditions

Interventions

TypeNameDescription
PROCEDUREdexmedetomidinepatients will recieve moderate sedation by dexmedetomidine as study group
PROCEDUREgeneral anesthesiageneral anesthesia with neuromuscular blockade under controlled ventilation as control group.

Timeline

Start date
2023-04-01
Primary completion
2023-10-01
Completion
2023-10-01
First posted
2023-03-23
Last updated
2023-10-25

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT05781035. Inclusion in this directory is not an endorsement.