Clinical Trials Directory

Trials / Completed

CompletedNCT02148432

Establishment of Ideal IV Sedative Regimen for Successful Fiberoptic Bronchoscopy in Assessing the Site, Severity of Sleep Apnea Syndrome

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
31 (actual)
Sponsor
Yonsei University · Academic / Other
Sex
All
Age
20 Years – 60 Years
Healthy volunteers
Accepted

Summary

Venous thromboembolism(VTE) is the third most common cardiovascular complication among hospitalized patients, and can even cause death. VTE often occurs in intensive care patients and there had been many efforts to prevent such complication. The American College of Chest Physicians (ACCP) had published evidence-based clinical practice guideline for VTE prophylaxis. This study focuses on how VTE prophylaxis is being performed in both medical and surgical ICUs in a single University hospital, and sees the differences in such prophylactic patterns.

Conditions

Interventions

TypeNameDescription
DRUGdexmedetomidine infusion rate, 0.5 mcg/kg/hrcontinuous infusion of dexmedetomidine at rate of 0.5 mcg/kg/hr
DRUGdexmedetomidine infusion rate, 1.0 mcg/kg/hrcontinuous infusion of dexmedetomidine at rate of 1.0 mcg/kg/hr

Timeline

Start date
2014-05-19
Primary completion
2016-04-29
Completion
2016-04-29
First posted
2014-05-28
Last updated
2017-01-25

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT02148432. Inclusion in this directory is not an endorsement.

Establishment of Ideal IV Sedative Regimen for Successful Fiberoptic Bronchoscopy in Assessing the Site, Severity of Sle (NCT02148432) · Clinical Trials Directory