Comparison of programmed intermittent epidural bolus injection and continuous epidural injection in controlling night pain and improving sleep quality after thoracotomy
Not Applicable
Completed
- Conditions
- Diseases of the respiratory system
- Registration Number
- KCT0005198
- Lead Sponsor
- Pusan National University Yangsan Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 76
Inclusion Criteria
Patients who are scheduled for thoracotomy due to lung cancer or other lung disease, who are American Society of Anesthesiology physical status I-III and over 19 years old.
Exclusion Criteria
Patients with difficult coordination, patients with blood clotting deficiencies, those with neurological defects at the treatment site, patients with allergic reactions to levobupivacaine in previous surgery or procedures, pregnant women are excluded.
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Postoperative pain score
- Secondary Outcome Measures
Name Time Method If pain control is poor, the total amount of pain medication administered, the frequency of administration, and the time of administration.;Subject's sleep quality;Patient satisfaction with pain control;Pattern of use of portable electronic injection pump in subjects for 48 hours after surgery