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NCT01542645 · ClinicalTrials.gov registry record · Phase 4

The Effect of Choice of Intraoperative Opioid on Postoperative Pain

A Phase 4 study, sponsored by Endeavor Health.

Completed
Registry status
Phase 4
Development phase
164
Enrollment target

NCT01542645 is a Phase 4 study that has completed, run by Endeavor Health. The registered enrollment target is 164 participants.

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The verdict

NCT01542645, a Phase 4 study, has completed, sponsored by Endeavor Health.

COMPLETED
Registry status
Phase 4
Development phase
164 participants
Enrollment target

Study Summary

The primary aim of this randomized, double-blind study is to examine the effect of a single intraoperative dose of methadone on postoperative pain and analgesic requirements in patients undergoing cardiac surgery with cardiopulmonary bypass. These patients will be compared to subjects receiving a standard dose of the "traditional" intraoperative opioid (fentanyl). Secondary outcome measures to be assessed will include standard recovery variables (such as length of postoperative intubation, ICU length of stay, incidence of nausea or vomiting, level of sedation). In addition, patients will be assessed for the development of chronic postoperative pain.

Interventions

  • DRUG Methadone
  • DRUG Fentanyl

Trial Details

FieldValue
Enrollment Target 164 participants
Start Date 2010-09
Est. Completion 2014-09
Phase Phase 4

Sponsor

Endeavor Health

94 total trials

What the Registry Record Tells You About NCT01542645

The ClinicalTrials.gov registry entry for NCT01542645 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 164 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Endeavor Health, which has 94 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which Methadone is the first listed.

NCT01542645 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT01542645 about?

NCT01542645 is a clinical study titled "The Effect of Choice of Intraoperative Opioid on Postoperative Pain". The primary aim of this randomized, double-blind study is to examine the effect of a single intraoperative dose of methadone on postoperative pain and analgesic requirements in patients undergoing cardiac surgery with cardiopulmonary bypass. These patients will be compared to subjects receiving a st...

What is the current status of trial NCT01542645?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 164 participants. The study started on 2010-09. Estimated completion is 2014-09.

What interventions are being tested in trial NCT01542645?

The interventions under investigation include: Methadone (DRUG), Fentanyl (DRUG).

Who is sponsoring clinical trial NCT01542645?

This trial is sponsored by Endeavor Health, which has 94 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.