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Intranasal vs. IV Dexmedetomidine in Endoscopic Sinus Surgery

NCT05595083 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 54

Last updated 2023-09-06

No results posted yet for this study

Summary

The aim of this study is to compare intranasal dexmedetomidine versus intravenous dexmedetomidine for improving the quality of the operative field in Functional endoscopic sinus surgery (FESS).

Conditions

  • Functional Endoscopic Sinus Surgery
  • Dexmedetomidine

Interventions

DRUG

intranasal dexmedetomidine group

patients will receive 1.5 ug/kg intranasal dexmedetomidine diluted with saline + infusion saline

DRUG

intravouns dexmedetomidine group

patients will receive 0.1- 0.4 ug/kg intravenous infusion dexmedetomidine + intranasal saline.

Sponsors & Collaborators

  • Kafrelsheikh University

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2022-11-01
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 NCT05595083 on ClinicalTrials.gov