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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02130544
Other study ID # 201403039RIND
Secondary ID
Status Recruiting
Phase N/A
First received May 1, 2014
Last updated December 3, 2014
Start date November 2014
Est. completion date April 2015

Study information

Verified date December 2014
Source National Taiwan University Hospital
Contact Fu-Lan Chuang
Phone +886-953358755
Email uniques3146@yahoo.com.tw
Is FDA regulated No
Health authority Taiwan: Department of Health
Study type Observational

Clinical Trial Summary

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态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.


Recruitment information / eligibility

Status Recruiting
Enrollment 150
Est. completion date April 2015
Est. primary completion date April 2015
Accepts healthy volunteers No
Gender Both
Age group 20 Years and older
Eligibility Inclusion Criteria:

1. Age >= 20

2. Using intravenous patient-controlled analgesia for postoperative analgesia

3. ASA physical status classification I-III

Exclusion Criteria:

1. Staying in intensive care unit after surgery

2. Emergency surgery

3. Pregnancy

4. Other surgery incisions which are not used for the video-assisted thoracoscopic surgery

5. Patients never use intravenous patient-controlled analgesia after surgery

Study Design

Observational Model: Cohort, Time Perspective: Retrospective


Related Conditions & MeSH terms


Locations

Country Name City State
Taiwan National Taiwan University Hospital Taipei

Sponsors (1)

Lead Sponsor Collaborator
National Taiwan University Hospital

Country where clinical trial is conducted

Taiwan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Postoperative pain scale postoperative day 1 to day 3 Yes
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