CClinicalTrials.gg
Status unknownNCT01527890Updated Feb 7, 2012

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

An observational study in Nausea and Vomiting, sponsored by Yonsei University. Status unknown at 1 site in Korea, Republic of. Open to participants aged 20 Years to 60 Years. Per ClinicalTrials.gov, last updated 2012-02-07.

Sponsored by Yonsei University · Observational

The sponsor has not verified this record recently (last verified Feb 2012), so the status shown — last known as Recruiting — may be out of date.
Study type
Observational
Model
Cohort
Time perspective
Retrospective
Enrollment
2,000
Ages
20 Years to 60 Years
Sex
All
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Study 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).

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Conditions studied

  • Nausea
  • Vomiting

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Keywords

  • intravenous patient-controlled analgesia
  • IV PCA
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In context

Vomiting

1,100 studies on the registry are indexed under Vomiting; 134 are open to participants now.

This study's planned enrollment of 2,000 is above the median of 160 across 124 observational studies indexed under Vomiting.

Browse Vomiting studies →

Lead sponsor

Yonsei University is the lead sponsor of 1,387 studies on the registry; 232 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
20 Years to 60 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Patients with Intravenous Fentanyl Patient-controlled Analgesia for postoperative pain control

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

Exclusion Criteria:

  1. Reoperation within 48 hours
  2. Patients who cannot express numerical rating scale for pain due to sedation
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Study design

Observational model
Cohort
Time perspective
Retrospective
Enrollment
2,000 participants (estimated)

Interventions

  • DrugFentanyl

    intravenous patient-controlled analgesia

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Study locations

1 of 1 sites recruiting
  • Gangnam Severance Hospital
    Seoul, 125-070, Korea, Republic of
    Recruiting
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 7, 2012, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT01527890
Lead sponsor
Yonsei University
Responsible party
Yon Hee Shim (Yonsei University College of Medicine, Yonsei University) — Principal investigator
First posted
Feb 7, 2012
Start date
Feb 2012
Primary completion
Sep 2012 (estimated)
Completion
Oct 2012 (estimated)
Last update
Feb 7, 2012

Study contacts

Yon Hee Shim, MD, PhD
Contact
tren125@yuhs.ac
82-2-2019-3547 ext. 3547
Jong Bum Choi, MD
Contact
romeojb@naver.com
82-2-2019-3528
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Feb 2012. You cannot join it, but the record below documents what was studied.

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