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Analgesic Effect of Intravenous Patient-Controlled Analgesia (IV PCA) Versus Paravertebral Block After Video Assisted Thoracic Surgery (VATS)

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT01538914
First Posted: February 24, 2012
Last Update Posted: April 20, 2016
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
Jae-Hyon Bahk, MD, PhD, Seoul National University Hospital
February 16, 2012
February 24, 2012
April 20, 2016
February 2013
February 2015   (Final data collection date for primary outcome measure)
severity of acute postoperative pain when moving [ Time Frame: 24 hours after VATS ]
Same as current
Complete list of historical versions of study NCT01538914 on ClinicalTrials.gov Archive Site
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Analgesic Effect of Intravenous Patient-Controlled Analgesia (IV PCA) Versus Paravertebral Block After Video Assisted Thoracic Surgery (VATS)
A Comparison Between the Analgesic Effect of Intravenous Patient-controlled Analgesia and of Paravertebral Block After Video Assisted Thoracoscopic Surgery
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.
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Interventional
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Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Postoperative Pain After Video Assisted Thoracic Surgery
  • Procedure: paravertebral block
    Postoperative pain is controlled with local analgesics via PVB.
  • Procedure: PCA
    Postoperative pain is controlled with intravenous PCA.
  • Experimental: PVB
    Postoperative pain is controlled with local analgesics delivered via PVB.
    Intervention: Procedure: paravertebral block
  • Active Comparator: PCA
    Postoperatve pain is controlled with intravenous PCA.
    Intervention: Procedure: PCA
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
76
October 2015
February 2015   (Final data collection date for primary outcome measure)

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
Sexes Eligible for Study: All
20 Years to 70 Years   (Adult, Senior)
No
Contact information is only displayed when the study is recruiting subjects
Korea, Republic of
 
 
NCT01538914
JHBahk_VATS PVB
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Not Provided
Not Provided
Jae-Hyon Bahk, MD, PhD, Seoul National University Hospital
Seoul National University Hospital
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Not Provided
Seoul National University Hospital
April 2016

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP