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NCT06266364 · ClinicalTrials.gov registry record · NA

Targeted Plasticity Therapy for PTSD

A NA study of PTSD - Post Traumatic Stress Disorder, sponsored by The University of Texas at Dallas.

Recruiting
Registry status
NA
Development phase
20
Enrollment target
3
Study locations

NCT06266364 is a NA study of PTSD - Post Traumatic Stress Disorder that is actively recruiting participants, run by The University of Texas at Dallas. The registered enrollment target is 20 participants, below the 278-participant average among 14 other PTSD - Post Traumatic Stress Disorder trials with a reported enrollment target (93% lower). The trial reports 3 study locations across 1 state.

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The verdict

NCT06266364, a NA study of PTSD - Post Traumatic Stress Disorder, is actively recruiting participants, sponsored by The University of Texas at Dallas.

RECRUITING
Registry status
NA
Development phase
20 participants
Enrollment target
3
Study locations

Study Summary

Objectives of this study are to provide continued safety assessment for the ReStore system, and to gain further estimates of the effect size of Vagus Nerve Stimulation (VNS) therapy with Prolonged Exposure Therapy (PE) compared to PE with placebo (sham) stimulation in participants with posttraumatic stress disorder (PTSD)

Conditions Studied

PTSD - Post Traumatic Stress Disorder

Interventions

  • DEVICE Active VNS stimulation
  • DEVICE Sham VNS stimulation

Study Locations (3)

Texas

  • The University of Texas Health Austin Ambulatory Surgery Center - Austin
  • Baylor University Medical Center - Dallas
  • Texas Biomedical Device Center - Richardson

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2024-12-30
Est. Completion 2028-06
Phase NA

Sponsor

The University of Texas at Dallas

50 total trials

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What the Registry Record Tells You About NCT06266364

The ClinicalTrials.gov registry entry for NCT06266364 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 20 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 278-participant average among 14 other PTSD - Post Traumatic Stress Disorder trials with a reported enrollment target (93% lower). The listed sponsor is The University of Texas at Dallas, which has 50 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with PTSD - Post Traumatic Stress Disorder appearing as the primary indexed condition, and to 2 interventions - of which Active VNS stimulation is the first listed.

NCT06266364 reports 3 study locations spanning 1 distinct geographic area - top geographies include Texas.

Frequently Asked Questions

What is clinical trial NCT06266364 about?

NCT06266364 is a clinical study titled "Targeted Plasticity Therapy for PTSD". Objectives of this study are to provide continued safety assessment for the ReStore system, and to gain further estimates of the effect size of Vagus Nerve Stimulation (VNS) therapy with Prolonged Exposure Therapy (PE) compared to PE with placebo (sham) stimulation in participants with posttraumatic...

What is the current status of trial NCT06266364?

This trial is currently recruiting. It is a NA study. The enrollment target is 20 participants. The study started on 2024-12-30. Estimated completion is 2028-06.

What conditions does trial NCT06266364 study?

This clinical trial studies the following conditions: PTSD - Post Traumatic Stress Disorder.

What interventions are being tested in trial NCT06266364?

The interventions under investigation include: Active VNS stimulation (DEVICE), Sham VNS stimulation (DEVICE).

Who is sponsoring clinical trial NCT06266364?

This trial is sponsored by The University of Texas at Dallas, which has 50 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06266364 being conducted?

This trial has 3 study locations across Texas. 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.