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Effect of Additive Lorazepam on Patient Satisfaction as a Premedication in Diagnostic Flexible Bronchoscopy

Effect of Additive Lorazepam on Patient Satisfaction as a Premedication in Diagnostic Flexible Bronchoscopy

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01121055
Enrollment
372
Registered
2010-05-12
Start date
2010-03-31
Completion date
2010-12-31
Last updated
2010-05-31

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

Conditions

Patient Satisfaction for Bronchoscopy

Keywords

Fiberoptic Bronchoscopy, Patient, Satisfaction, Lorazepam

Brief summary

Many patients undergoing flexible bronchoscopy (FB) experience anxiety and discomfort during the procedure. The investigators want to evaluate whether an additional Lorazepam premedication would improve patient satisfaction for FB.

Detailed description

The enrolled patients are randomized to either the control or Lorazepam groups according to a random sample chart of numbers. The patients complete questionnaires about baseline anxiety level and satisfaction for FB within 24 hours after the FB.

Interventions

DRUGLorazepam

Lorazepam 0.5mg po at night one day before FB and Lorazepam 1mg po 30min before the FB

DRUGControl

Placebo 1T po at night one day before FB and placebo 1T po 30min before the FB

Sponsors

Seoul National University Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Adult patients (aged 18 years or older) admitted to the Respiratory Department

Exclusion criteria

* outpatient procedures * therapeutic bronchoscopy * expected operation or discharge within 24 hours after the FB * sedative premedication * endotracheal intubation with mechanical ventilation * inability to speak Korean

Design outcomes

Primary

MeasureTime frame
patient satisfactionwithin 24 hr of bronchoscopy

Secondary

MeasureTime frame
relationship between patient satisfaction and sleep quality, anxiety level24hr before and after bronchoscopy

Countries

South Korea

Contacts

Primary ContactSeok-Chul Yang, MD, PhD
scyang@snu.ac.kr+82-2-2072-0354
Backup ContactJong Sun Park, MD
jspark.im@gmail.com

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026