Analgesic Effect of Intravenous Patient-Controlled Analgesia (IV PCA) Versus Paravertebral Block After Video Assisted Thoracic Surgery (VATS)
This study is currently recruiting participants.
Verified February 2012 by Seoul National University Hospital
Sponsor:
Seoul National University Hospital
Information provided by (Responsible Party):
Jae-Hyon Bahk, Seoul National University Hospital
ClinicalTrials.gov Identifier:
NCT01538914
First received: February 16, 2012
Last updated: February 23, 2012
Last verified: February 2012
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Purpose
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.
| Condition | Intervention |
|---|---|
|
Postoperative Pain After Video Assisted Thoracic Surgery |
Procedure: paravertebral block Procedure: PCA |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Parallel Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | A Comparison Between the Analgesic Effect of Intravenous Patient-controlled Analgesia and of Paravertebral Block After Video Assisted Thoracoscopic Surgery |
Further study details as provided by Seoul National University Hospital:
Primary Outcome Measures:
- severity of acute postoperative pain when moving [ Time Frame: 24 hours after VATS ] [ Designated as safety issue: No ]
| Estimated Enrollment: | 76 |
| Study Start Date: | February 2012 |
| Estimated Primary Completion Date: | February 2013 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: PVB
Postoperative pain is controlled with local analgesics delivered via PVB.
|
Procedure: paravertebral block
Postoperative pain is controlled with local analgesics via PVB.
|
|
Active Comparator: PCA
Postoperatve pain is controlled with intravenous PCA.
|
Procedure: PCA
Postoperative pain is controlled with intravenous PCA.
|
Eligibility| Ages Eligible for Study: | 20 Years to 70 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Criteria
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
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01538914
Contacts
| Contact: Jae-Hyon Bahk, MD, PhD | 82-2-2072-2818 | bahkjh@snu.ac.kr |
Locations
| Korea, Republic of | |
| Seoul National University Hospital | Recruiting |
| Seoul, Korea, Republic of | |
| Contact: Jae Hyon Bahk, MD, PhD 82-2-2072-2818 bahkjh@snu.ac.kr | |
Sponsors and Collaborators
Seoul National University Hospital
More Information
No publications provided
| Responsible Party: | Jae-Hyon Bahk, Professor, Seoul National University Hospital |
| ClinicalTrials.gov Identifier: | NCT01538914 History of Changes |
| Other Study ID Numbers: | JHBahk_VATS PVB |
| Study First Received: | February 16, 2012 |
| Last Updated: | February 23, 2012 |
| Health Authority: | Korea: Food and Drug Administration |
Additional relevant MeSH terms:
|
Pain, Postoperative Postoperative Complications Pathologic Processes Pain Signs and Symptoms Analgesics |
Sensory System Agents Peripheral Nervous System Agents Physiological Effects of Drugs Pharmacologic Actions Central Nervous System Agents Therapeutic Uses |
ClinicalTrials.gov processed this record on June 18, 2013