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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01538914
Other study ID # JHBahk_VATS PVB
Secondary ID
Status Completed
Phase N/A
First received February 16, 2012
Last updated April 19, 2016
Start date February 2013
Est. completion date October 2015

Study information

Verified date April 2016
Source Seoul National University Hospital
Contact n/a
Is FDA regulated No
Health authority Korea: Food and Drug Administration
Study type Interventional

Clinical Trial Summary

The purpose of this study is to compare the analgesic effect of paravertebral block with that of intravenous patient-controlled analgesia after video assisted thoracic surgery.


Recruitment information / eligibility

Status Completed
Enrollment 76
Est. completion date October 2015
Est. primary completion date February 2015
Accepts healthy volunteers No
Gender Both
Age group 20 Years to 70 Years
Eligibility Inclusion Criteria:

- patients receiving video assisted thoracic surgery

Exclusion Criteria:

- patients with cardiovascular disease

- patients with neurologic disease

- patients with contraindications to paravertebral block or epidural block

- patients with history of previous VATS

- patients with pain at the expected incision site

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Procedure:
paravertebral block
Postoperative pain is controlled with local analgesics via PVB.
PCA
Postoperative pain is controlled with intravenous PCA.

Locations

Country Name City State
Korea, Republic of Seoul National University Hospital Seoul

Sponsors (1)

Lead Sponsor Collaborator
Seoul National University Hospital

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary severity of acute postoperative pain when moving 24 hours after VATS No