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NCT03417960 · ClinicalTrials.gov registry record · NA

Accelerated iTBS for Post Partum Depression

A NA study of Post Partum Depression, sponsored by Medical University of South Carolina.

Recruiting
Registry status
NA
Development phase
40
Enrollment target
1
Study location

NCT03417960 is a NA study of Post Partum Depression that is actively recruiting participants, run by Medical University of South Carolina. The registered enrollment target is 40 participants, below the 231-participant average among 9 other Post Partum Depression trials with a reported enrollment target (83% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT03417960, a NA study of Post Partum Depression, is actively recruiting participants, sponsored by Medical University of South Carolina.

RECRUITING
Registry status
NA
Development phase
40 participants
Enrollment target
1
Study location

Study Summary

Study 1: The investigators are studying the feasibility and tolerability of 10x/day intermittent theta burst (excitatory) transcranial magnetic stimulation to the left dorsolateral prefrontal cortex over the course of 6 days for women with post-partum depression. The investigators further aim to characterize the anticipated anti-depressant effect of this treatment paradigm. Study 2: The investigators are studying the feasibility and tolerability of 12 sessions/day of intermittent theta burse (excitatory) transcranial magnetic stimulation to the left dorsolateral prefrontal cortex over 5 days for women with post-partum depression. The investigators aim to compare the two different treatment schedules.

Conditions Studied

Post Partum Depression

Interventions

  • DEVICE iTBS

Study Locations (1)

South Carolina

  • Medical University of South Carolina - Charleston

Trial Details

FieldValue
Enrollment Target 40 participants
Start Date 2018-01-24
Est. Completion 2027-08-30
Phase NA

Sponsor

Medical University of South Carolina

755 total trials

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What the Registry Record Tells You About NCT03417960

The ClinicalTrials.gov registry entry for NCT03417960 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 40 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 231-participant average among 9 other Post Partum Depression trials with a reported enrollment target (83% lower). The listed sponsor is Medical University of South Carolina, which has 755 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Post Partum Depression appearing as the primary indexed condition, and to 1 intervention - of which iTBS is the first listed.

NCT03417960 reports 1 study location spanning 1 distinct geographic area - top geographies include South Carolina.

Frequently Asked Questions

What is clinical trial NCT03417960 about?

NCT03417960 is a clinical study titled "Accelerated iTBS for Post Partum Depression". Study 1: The investigators are studying the feasibility and tolerability of 10x/day intermittent theta burst (excitatory) transcranial magnetic stimulation to the left dorsolateral prefrontal cortex over the course of 6 days for women with post-partum depression. The investigators further aim to cha...

What is the current status of trial NCT03417960?

This trial is currently recruiting. It is a NA study. The enrollment target is 40 participants. The study started on 2018-01-24. Estimated completion is 2027-08-30.

What conditions does trial NCT03417960 study?

This clinical trial studies the following conditions: Post Partum Depression.

What interventions are being tested in trial NCT03417960?

The interventions under investigation include: iTBS (DEVICE).

Who is sponsoring clinical trial NCT03417960?

This trial is sponsored by Medical University of South Carolina, which has 755 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT03417960 being conducted?

This trial has 1 study location across South Carolina. 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.