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NCT06317636 · ClinicalTrials.gov registry record · Phase 4

Propofol-Enhanced Assessment of Ketamine for Chronic Pain and Depression

A Phase 4 study of Depression and Chronic Pain, sponsored by Stanford University.

Active
Registry status
Phase 4
Development phase
40
Enrollment target
1
Study location

NCT06317636 is a Phase 4 study of Depression and Chronic Pain that is active but no longer recruiting, run by Stanford University. The registered enrollment target is 40 participants, below the 786-participant average among 679 other Depression trials with a reported enrollment target (95% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT06317636, a Phase 4 study of Depression and Chronic Pain, is active but no longer recruiting, sponsored by Stanford University.

ACTIVE NOT RECRUITING
Registry status
Phase 4
Development phase
40 participants
Enrollment target
1
Study location

Study Summary

The goal of this clinical trial is to compare ketamine to a placebo when given as a single infusion during IV sedation in adults with chronic pain and depression. We do not know whether ketamine will be more effective than placebo under these circumstances. This study aims to: * Evaluate whether placebo is non-inferior to ketamine in treating chronic pain and depression, when delivered under propofol sedation * Confirm that propofol sedation is a safe way to keep participants blinded to treatment * Assess patients' comfort with the sedation process to improve future studies * Explore whether patient expectations affects their pain and depression Participants will: * Need to qualify for the study based on stringent medical criteria * Undergo sedation with propofol * Randomly receive either a ketamine or a placebo (saline) infusion during sedation * Complete several study assessments over 5-7 weeks

Conditions Studied

Interventions

  • DRUG Ketamine
  • DRUG Normal saline

Study Locations (1)

California

  • Stanford University - Stanford

Trial Details

FieldValue
Enrollment Target 40 participants
Start Date 2025-01-28
Est. Completion 2026-12
Phase Phase 4

Sponsor

Stanford University

1,744 total trials

What the Registry Record Tells You About NCT06317636

The ClinicalTrials.gov registry entry for NCT06317636 describes a study currently listed as active not recruiting, categorized as Phase 4. The registered enrollment target is 40 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 786-participant average among 679 other Depression trials with a reported enrollment target (95% lower). The listed sponsor is Stanford University, which has 1,744 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Depression appearing as the primary indexed condition, and to 2 interventions - of which Ketamine is the first listed.

NCT06317636 reports 1 study location spanning 1 distinct geographic area - top geographies include California.

Frequently Asked Questions

What is clinical trial NCT06317636 about?

NCT06317636 is a clinical study titled "Propofol-Enhanced Assessment of Ketamine for Chronic Pain and Depression". The goal of this clinical trial is to compare ketamine to a placebo when given as a single infusion during IV sedation in adults with chronic pain and depression. We do not know whether ketamine will be more effective than placebo under these circumstances. This study aims to: * Evaluate whether p...

What is the current status of trial NCT06317636?

This trial is currently active not recruiting. It is a Phase 4 study. The enrollment target is 40 participants. The study started on 2025-01-28. Estimated completion is 2026-12.

What conditions does trial NCT06317636 study?

This clinical trial studies the following conditions: Depression, Chronic Pain.

What interventions are being tested in trial NCT06317636?

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

Who is sponsoring clinical trial NCT06317636?

This trial is sponsored by Stanford University, which has 1,744 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06317636 being conducted?

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

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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.