Comparison of programmed intermittent epidural bolus injection and continuous epidural injection in controlling night pain and improving sleep quality after thoracotomy

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0005198

Enrollment

Registered

2020-07-03

Start date

2020-06-22

Completion date

Unknown

Last updated

2021-08-30

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

Conditions

None listed

Interventions

Procedure/Surgery : In order to control postoperative pain, patient controlled analgesia using thoracic epidural block is applied to T6-T9 levels in both groups. The study subjects were divided into a

Eligibility

Sex/Gender

All

Inclusion criteria

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

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.

Design outcomes

Primary

Measure	Time frame
Postoperative pain score	—

Secondary

Measure	Time frame
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	—

Countries

Korea, Republic of

Contacts

Public ContactGyeong-Jo Byeon

Pusan National University Yangsan Hospital

cooki1713@naver.com+82-55-360-2758

Outcome results