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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT01527890
Other study ID # 3-2011-0238
Secondary ID
Status Recruiting
Phase N/A
First received January 27, 2012
Last updated February 2, 2012
Start date February 2012
Est. completion date October 2012

Study information

Verified date February 2012
Source Yonsei University
Contact Yon Hee Shim, MD, PhD
Phone 82-2-2019-3547
Email tren125@yuhs.ac
Is FDA regulated No
Health authority Korea: Food and Drug Administration
Study type Observational

Clinical Trial Summary

In this retrospective study, the investigators examined incidence and risk factors of postoperative nausea and vomiting (PONV) in patients with fentanyl-based intravenous patient-controlled analgesia (IV-PCA).


Recruitment information / eligibility

Status Recruiting
Enrollment 2000
Est. completion date October 2012
Est. primary completion date September 2012
Accepts healthy volunteers No
Gender Both
Age group 20 Years to 60 Years
Eligibility Inclusion Criteria:

1. Adults between 20 to 60 years old

2. Date from 1st, May 2011 to 31st, October 2011

3. Patients with fentanyl based intravenous patient-controlled analgesia for postoperative pain control

Exclusion Criteria:

1. Reoperation within 48 hours

2. Patients who cannot express numerical rating scale for pain due to sedation

Study Design

Observational Model: Cohort, Time Perspective: Retrospective


Related Conditions & MeSH terms


Intervention

Drug:
Fentanyl
intravenous patient-controlled analgesia

Locations

Country Name City State
Korea, Republic of Gangnam Severance Hospital Seoul

Sponsors (1)

Lead Sponsor Collaborator
Yonsei University

Country where clinical trial is conducted

Korea, Republic of, 

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