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NCT03359395 · ClinicalTrials.gov registry record · Phase 4

Pre-medication With Alfentanil vs Placebo During ECT

A Phase 4 study, sponsored by Wake Forest University Health Sciences.

Completed
Registry status
Phase 4
Development phase
100
Enrollment target

NCT03359395: Completed Phase 4 study, sponsored by Wake Forest University Health Sciences.

NCT03359395 is a Phase 4 study that has completed, run by Wake Forest University Health Sciences. The registered enrollment target is 100 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (81% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03359395, a Phase 4 study, has completed, sponsored by Wake Forest University Health Sciences.

COMPLETED
Registry status
Phase 4
Development phase
100 participants
Enrollment target

Study Summary

Hemodynamic changes associated with the conduct of electroconvulsive therapy may be minimized with the administration of alfentanil as part of their anesthetic regimen. This study proposes to compare the effects in a blinded fashion. Currently alfentanil is an FDA approved drug used on a daily basis by anesthesiologists on other surgeries so this is not a new indication.

Primary Outcome

comparison of Systolic blood pressure changes alfentanil vs placebo

Interventions

  • DRUG Placebos
  • DRUG Alfentanil

Trial Details

FieldValue
Enrollment Target 100 participants
Start Date 2018-06-04
Est. Completion 2020-02-17
Phase Phase 4
Wake Forest University Health Sciences

1,140 total trials

What the finished NCT03359395 record still lists

NCT03359395 is an interventional study that assigns participants to a tested intervention. The registered 100 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 (81% lower).

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

NCT03359395 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03359395 about?

NCT03359395 is a clinical study titled "Pre-medication With Alfentanil vs Placebo During ECT". Hemodynamic changes associated with the conduct of electroconvulsive therapy may be minimized with the administration of alfentanil as part of their anesthetic regimen. This study proposes to compare the effects in a blinded fashion. Currently alfentanil is an FDA approved drug used on a daily basis...

What is the current status of trial NCT03359395?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 100 participants. The study started on 2018-06-04. Estimated completion is 2020-02-17.

What interventions are being tested in trial NCT03359395?

The interventions under investigation include: Placebos (DRUG), Alfentanil (DRUG).

Who is sponsoring clinical trial NCT03359395?

This trial is sponsored by Wake Forest University Health Sciences, which has 1,140 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03359395's enrollment target sits among peer trials

100 770th of 2000 higher than 1,148 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 NCT03359395, the US trial registry maintained by the National Library of Medicine. NCT03359395 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.