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

NCT05781035 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 70

Last updated 2023-10-25

No results posted yet for this study

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

Conditions

  • Sedation
  • Dexmedetomidine
  • EBUS Guided Transbronchial Needle Aspiration

Interventions

PROCEDURE

dexmedetomidine

patients will recieve moderate sedation by dexmedetomidine as study group

PROCEDURE

general anesthesia

general anesthesia with neuromuscular blockade under controlled ventilation as control group.

Sponsors & Collaborators

  • Kafrelsheikh University

    lead OTHER

Principal Investigators

  • Mohamed S Torky · Lecturer of Chest Department , Faculty of Medicine, Tanta University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-04-01
Primary Completion
2023-10-01
Completion
2023-10-01

Countries

  • Egypt

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05781035 on ClinicalTrials.gov