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NCT07233278

High-Intensity, Low-Frequency Periodic rTMS Over the Right Dorsolateral Prefrontal Cortex on Cardiac Autonomic Regulation in Women With Recurrent Pregnancy Loss and Anxiety

Not yet recruiting NA Last updated 18 November 2025
What this trial tests

NA trial testing Rhythmic repetitive transcranial magnetic stimulation (rTMS) at 120% RMT, 1 Hz, 60-s cycles in Recurrent Pregnancy Loss(RPL) in 46 participants. Not yet recruiting.

Timeline
20 November 2025
Primary endpoint
14 April 2026
20 April 2026

Quick facts

Lead sponsorShenyang Medical College
PhaseNA
StatusNot yet recruiting
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposetreatment
Enrollment46
Start date20 November 2025
Primary completion14 April 2026
Estimated completion20 April 2026
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Shenyang Medical College

Who can join

Adults 18 to 45, female only, with Recurrent Pregnancy Loss(RPL) or Anxiety. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The goal of this clinical trial is to determine whether high-intensity, low-frequency periodic repetitive transcranial magnetic stimulation (rTMS) applied to the right dorsolateral prefrontal cortex (DLPFC) can modulate cardiac autonomic regulation in women with recurrent pregnancy loss (RPL) and comorbid anxiety. The main questions it aims to answer are: Does 120% resting motor threshold (RMT) rhythmic low-frequency rTMS reduce heart rate during stimulation time windows compared with sham stimulation? Does 120% RMT rTMS alter heart-rate-variability (HRV) spectral power at the target frequency (0.0167 Hz) compared with sham stimulation? Researchers will compare active rTMS with sham rTMS to determine whether the active intervention produces measurable changes in cardiac autonomic activity. Participants will: Undergo a single session of rTMS or sham stimulation consisting of 20 consecutive stimulation time windows (each 60 seconds: 40 seconds of 1-Hz stimulation plus 20 seconds of rest) targeting the right DLPFC; Have continuous electrocardiography (ECG) recordings collected during the entire stimulation session; Complete clinical and psychiatric assessments before participation.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other Shenyang Medical College trials

Trials by the same sponsor.

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Data sources for this page

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