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NCT04831736 · ClinicalTrials.gov registry record · Phase 4

Effect of Postoperative Single Dose of Ketamine on Pain After Mastectomy

A Phase 4 study of Postoperative Pain, sponsored by NYU Langone Health.

Completed
Registry status
Phase 4
Development phase
31
Enrollment target
1
Study location

NCT04831736 is a Phase 4 study of Postoperative Pain that has completed, run by NYU Langone Health. The registered enrollment target is 31 participants, below the 231-participant average among 63 other Postoperative Pain trials with a reported enrollment target (87% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT04831736, a Phase 4 study of Postoperative Pain, has completed, sponsored by NYU Langone Health.

COMPLETED
Registry status
Phase 4
Development phase
31 participants
Enrollment target
1
Study location

Study Summary

This is a randomized, single blinded, placebo-controlled trial to study the effectiveness of a subanesthetic dose (0.6mg/kg) of ketamine versus placebo (saline) on postoperative pain on adult women undergoing mastectomy. The objective of the study is to examine the effect of a subanesthetic dose (0.6mg/kg) of ketamine vs. saline control on postoperative pain in subjects who have undergone mastectomy.

Conditions Studied

Postoperative Pain

Interventions

  • DRUG Placebo
  • DRUG Ketamine

Study Locations (1)

New York

  • NYU Langone Health - New York

Trial Details

FieldValue
Enrollment Target 31 participants
Start Date 2021-04-26
Est. Completion 2022-03-29
Phase Phase 4

Sponsor

NYU Langone Health

1,164 total trials

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What the Registry Record Tells You About NCT04831736

The ClinicalTrials.gov registry entry for NCT04831736 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 31 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 231-participant average among 63 other Postoperative Pain trials with a reported enrollment target (87% lower). The listed sponsor is NYU Langone Health, which has 1,164 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Postoperative Pain appearing as the primary indexed condition, and to 2 interventions - of which Placebo is the first listed.

NCT04831736 reports 1 study location spanning 1 distinct geographic area - top geographies include New York.

Frequently Asked Questions

What is clinical trial NCT04831736 about?

NCT04831736 is a clinical study titled "Effect of Postoperative Single Dose of Ketamine on Pain After Mastectomy". This is a randomized, single blinded, placebo-controlled trial to study the effectiveness of a subanesthetic dose (0.6mg/kg) of ketamine versus placebo (saline) on postoperative pain on adult women undergoing mastectomy. The objective of the study is to examine the effect of a subanesthetic dose (0...

What is the current status of trial NCT04831736?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 31 participants. The study started on 2021-04-26. Estimated completion is 2022-03-29.

What conditions does trial NCT04831736 study?

This clinical trial studies the following conditions: Postoperative Pain.

What interventions are being tested in trial NCT04831736?

The interventions under investigation include: Placebo (DRUG), Ketamine (DRUG).

Who is sponsoring clinical trial NCT04831736?

This trial is sponsored by NYU Langone Health, which has 1,164 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT04831736 being conducted?

This trial has 1 study location across New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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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.