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NCT02349152 · ClinicalTrials.gov registry record · Phase 4

Remifentanil and Glycemic Response in Cardiac Surgery

A Phase 4 study, sponsored by Kathirvel Subramaniam.

Completed
Registry status
Phase 4
Development phase
116
Enrollment target

NCT02349152: Completed Phase 4 study, sponsored by Kathirvel Subramaniam.

NCT02349152 is a Phase 4 study that has completed, run by Kathirvel Subramaniam. The registered enrollment target is 116 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (78% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02349152, a Phase 4 study, has completed, sponsored by Kathirvel Subramaniam.

COMPLETED
Registry status
Phase 4
Development phase
116 participants
Enrollment target

Study Summary

This study evaluates the effect of using remifentanil during cardiopulmonary bypass surgery to supress the hyperglycemic response in perioperative period. Half of the participants will receive continuous intravenous remifentanil during surgery, while the other half will receive intermittent intravenous fentanyl during surgery. Intermittent intravenous fentanyl administration is this institution's standard of care.

Primary Outcome

Percentage of patients with two or more intraoperative blood glucose levels greater than 180 mg/dl. Percentage in both groups will be estimated, then the difference in this statistic will form the primary outcome measure of this study. (Primary Outcome changed on 06/15/2015-Change Approved by University of Pittsburgh IRB on 06/22/2015- First patient enrolled January 2016)

Interventions

  • DRUG Fentanyl
  • DRUG Remifentanil

Trial Details

FieldValue
Enrollment Target 116 participants
Start Date 2016-01
Est. Completion 2017-12
Phase Phase 4
Kathirvel Subramaniam

5 total trials

What the finished NCT02349152 record still lists

NCT02349152 is an interventional study that assigns participants to a tested intervention. The registered 116 participants enrollment target is mid-sized for trials with a published cap, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (78% lower).

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

NCT02349152 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02349152 about?

NCT02349152 is a clinical study titled "Remifentanil and Glycemic Response in Cardiac Surgery". This study evaluates the effect of using remifentanil during cardiopulmonary bypass surgery to supress the hyperglycemic response in perioperative period. Half of the participants will receive continuous intravenous remifentanil during surgery, while the other half will receive intermittent intraven...

What is the current status of trial NCT02349152?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 116 participants. The study started on 2016-01. Estimated completion is 2017-12.

What interventions are being tested in trial NCT02349152?

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

Who is sponsoring clinical trial NCT02349152?

This trial is sponsored by Kathirvel Subramaniam, which has 5 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02349152's enrollment target sits among peer trials

116 714th of 2000 higher than 1,283 of 2,000 other Phase 4 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 4 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT02349152, the US trial registry maintained by the National Library of Medicine. NCT02349152 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.