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Dexmedetomidine Versus Propofol Sedation in Flexible Bronchoscopy: A Randomized Controlled Trial

Dexmedetomidine Versus Propofol Sedation in Flexible Bronchoscopy: A Randomized Controlled Trial

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04211298
Enrollment
100
Registered
2019-12-26
Start date
2019-12-01
Completion date
2020-08-01
Last updated
2019-12-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Sedation Complication

Brief summary

The study will evaluate clinical outcomes during bronchoscopy procedures with dexmedetomidine in comparison to propofol. The clinical outcomes that will be evaluated are: oxygen saturation, transcutaneous Pco2, blood pressure and complications

Interventions

DRUGDexmedetomidine

Dexmedetomidine will be used for sedation during bronchoscopy

DRUGPropofol

Propofol

Sponsors

Rabin Medical Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

Randomised controlled trial

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* All patients in the age group 18 to 70 years requiring flexible bronchoscopic evaluation of the airway in the Pulmonary institute at Rabin medical center

Exclusion criteria

* known or suspected allergy to any of the study drugs, seizure disorder, renal (with serum creatinine \> 2 mg/dL) or hepatic impairment (elevated liver enzymes \> 2 times normal), haemodynamic instability (bradycardia with HR \< 50 bpm or hypotension with SBP \< 90 mmHg), or seriously ill patients with American Society of Anesthesiologists' physical status above III

Design outcomes

Primary

MeasureTime frameDescription
number of de-saturation eventsDuring the procedureNumber of events during bronchoscopy when saturation level decreased under 90%
Oxygen saturation time < 90%During the procedureTotal time during the procedure that the oxygen saturation was under 90%

Countries

Israel

Contacts

Primary ContactBarak Pertzov, MD
pertzovb@gmail.com972548080196
Backup ContactMordechai Kramer, MD
Kremerm@clalit.org.il97239377224

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 12, 2026