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

Phase 4
Conditions
Patient Satisfaction for Bronchoscopy
Interventions
Drug: Control
Registration Number
NCT01121055
Lead Sponsor
Seoul National University Hospital
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.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
372
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

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
ControlControlPlacebo 1T by mouth (po) at night one day before FB and placebo 1T po 30min before the FB
LorazepamLorazepamLorazepam 0.5mg po at night one day before FB and Lorazepam 1mg po 30min before the FB
Primary Outcome Measures
NameTimeMethod
patient satisfactionwithin 24 hr of bronchoscopy
Secondary Outcome Measures
NameTimeMethod
relationship between patient satisfaction and sleep quality, anxiety level24hr before and after bronchoscopy

Trial Locations

Locations (1)

Seoul National University Hospital

🇰🇷

Seoul, Korea, Republic of

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