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Effect of Intravenous Patient-controlled Analgesia (IV-PCA) With Fentanyl in Adults for Acute Postoperative Pain Control

The recruitment status of this study is unknown. The completion date has passed and the status has not been verified in more than two years.
Verified February 2012 by Yon Hee Shim, Yonsei University.
Recruitment status was:  Recruiting
Sponsor:
ClinicalTrials.gov Identifier:
NCT01527890
First Posted: February 7, 2012
Last Update Posted: February 7, 2012
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):
Yon Hee Shim, Yonsei University
  Purpose
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).

Condition Intervention
Nausea Vomiting Drug: Fentanyl

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Retrospective

Resource links provided by NLM:


Further study details as provided by Yon Hee Shim, Yonsei University:

Estimated Enrollment: 2000
Study Start Date: February 2012
Estimated Study Completion Date: October 2012
Estimated Primary Completion Date: September 2012 (Final data collection date for primary outcome measure)
Intervention Details:
    Drug: Fentanyl
    intravenous patient-controlled analgesia
  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   20 Years to 60 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
Patients with Intravenous Fentanyl Patient-controlled Analgesia for postoperative pain control
Criteria

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
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01527890


Contacts
Contact: Yon Hee Shim, MD, PhD 82-2-2019-3547 ext 3547 tren125@yuhs.ac
Contact: Jong Bum Choi, MD 82-2-2019-3528 romeojb@naver.com

Locations
Korea, Republic of
Gangnam Severance Hospital Recruiting
Seoul, Korea, Republic of, 125-070
Contact: Yon Hee Shim, MD, PhD    82-2-2019-3547 ext 3547    tren125@yuhs.ac   
Sponsors and Collaborators
Yonsei University
  More Information

Responsible Party: Yon Hee Shim, Yonsei University College of Medicine, Yonsei University
ClinicalTrials.gov Identifier: NCT01527890     History of Changes
Other Study ID Numbers: 3-2011-0238
First Submitted: January 27, 2012
First Posted: February 7, 2012
Last Update Posted: February 7, 2012
Last Verified: February 2012

Keywords provided by Yon Hee Shim, Yonsei University:
intravenous patient-controlled analgesia
IV PCA

Additional relevant MeSH terms:
Vomiting
Signs and Symptoms, Digestive
Signs and Symptoms
Fentanyl
Analgesics, Opioid
Narcotics
Central Nervous System Depressants
Physiological Effects of Drugs
Analgesics
Sensory System Agents
Peripheral Nervous System Agents
Adjuvants, Anesthesia
Anesthetics, Intravenous
Anesthetics, General
Anesthetics