- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02130544
Acute Pain Management Following Video-assisted Thoracoscopic Surgery: Comparison of Lobectomy and Wedge Resection
December 3, 2014 updated by: National Taiwan University Hospital
Viedo-assisted thoracoscopic surgery(VATS) have became popular in recent years.
There is no golden rule of postoperative analgesia for VATS.
Compared with lobectomy, wedge resection preserves better pulmonary function and is suitable for elder patients and patients who could not afford to have lobectomy.
In addition to surgery time、recovery time and hospital stay, wound incisions and organization damages are different,too.
Will patients also have different response to pain control after these two surgery?
The retrospective study is to compared the differences of postoperative pain management between VATS lobectomy and wedge resection.
Study Overview
Status
Unknown
Conditions
Study Type
Observational
Enrollment (Anticipated)
150
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
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Taipei, Taiwan
- Recruiting
- National Taiwan University Hospital
-
Contact:
- Ya-Jung cheng
- Phone Number: 65523 +886-2-2312-3456
- Email: chengyj@ntu.edu.tw
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
16 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Selected patients are from the hospital patients who are arranged to have video-assisted thoracoscopic surgery for lobectomy or wedge resection
Description
Inclusion Criteria:
- Age >= 20
- Using intravenous patient-controlled analgesia for postoperative analgesia
- ASA physical status classification I-III
Exclusion Criteria:
- Staying in intensive care unit after surgery
- Emergency surgery
- Pregnancy
- Other surgery incisions which are not used for the video-assisted thoracoscopic surgery
- Patients never use intravenous patient-controlled analgesia after surgery
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Retrospective
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Postoperative pain scale
Time Frame: postoperative day 1 to day 3
|
postoperative day 1 to day 3
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Ya-Jung Cheng, National Taiwan University Hospital
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
November 1, 2014
Primary Completion (Anticipated)
April 1, 2015
Study Completion (Anticipated)
April 1, 2015
Study Registration Dates
First Submitted
May 1, 2014
First Submitted That Met QC Criteria
May 2, 2014
First Posted (Estimate)
May 5, 2014
Study Record Updates
Last Update Posted (Estimate)
December 5, 2014
Last Update Submitted That Met QC Criteria
December 3, 2014
Last Verified
December 1, 2014
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 201403039RIND
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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