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Scientists zap brain in 12 people to map electrical reactions

NCT ID NCT07179224

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This completed study looked at how the brain's electrical activity changes when a magnetic stimulation device (rTMS) is applied to different spots on the forehead. Twelve adults each received one treatment session while their brain waves were recorded with EEG. The goal was simply to understand the brain's immediate response, not to treat any condition.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
transcranial magnetic stimulation (rTMS) device
What this could lead to
If successful, this could help refine how rTMS is delivered for conditions like depression or anxiety.
What could go wrong
This was a very small, early-stage study with only 12 participants. It measured brain activity, not treatment effects, so it may not lead to any direct clinical benefit.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

12 people

The number who actually took part.

Started

Sep 2025

Finished

Oct 2025

Lead sponsor

A company

The lead sponsor is a pharmaceutical, biotech, or medical-device company.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

20 years and older

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Age \> 19 years * Ability to determine the motor threshold of the participant. * Willingness to maintain on pre-study psychotherapeutic regime, and prescribed medications at a stable therapeutic dosage for at least 2 months prior to study entry. * Willingness to comply with study instructions and to return to the clinic for the required visits * Willingness to undergo EEG examination and proceed with the instructions from the study staff during the measurement * Women of child-bearing potential are required to use birth control measures during the whole duration of the study Exclusion Criteria: * electronic implants (Implanted stimulator devices in or near the head - rTMS devices are contraindicated for use in patients who have active or inactive implants including device leads, deep brain stimulators, cochlear implants, ocular implants, and vagus nerve stimulators, implanted devices such as cardiac pacemakers, defibrillators, and neurostimulators.), * metallic, ferromagnetic or other magnetic-sensitive implants/objects in or near the head\*, * application in the heart area, * persons with a tendency to seizure (hypotonic, epileptic), * ongoing anticoagulation therapy, * ongoing severe or life-threatening condition, * ongoing renal dialysis therapy or decompensated\*\* renal insufficiency, * decompensated\* hemorrhagic conditions, blood coagulation disorders, cardiovascular diseases, * malignant or benign tumour (within 30 cm of the treatment coil), * fever, * application over or in the near proximity (within 30 cm of the treatment coil) of tattoos with metallic ink * pregnancy or nursing * suicidal tendencies or recent attempt to commit suicide, * concurrent use of electroconvulsive therapy or vagus nerve stimulation, * ongoing or recent changes (less than 60 days) in intake doses of any pharmaceutical - products, standalone or in combination, that might lower the threshold of seizure potential, * ongoing withdrawal conditions from any dependence substance or medication associated with altered seizure risk history, * a psychotic disorder, including schizoaffective disorder, bipolar disease, or major depression with psychotic features, * history of primary or secondary tumors in CNS, cerebral aneurysm, * history of increased intracranial pressure or head trauma with loss of consciousness. * any medication that may alter EEG report (such as benzodiazepines, barbiturates, carbamazepine, valproate, phenothiazines, clozapine, tricyclic antidepressants, lithium, etc.), any other disease or condition at the investigator discretion that may pose risk to the patient or compromise the study * rTMS devices are contraindicated for use in patients who have conductive, ferromagnetic or other magnetic-sensitive metals implanted in their head (with some exceptions in the mouth - standard amalgam dental fillings, single post dental implants, and dental bridge work. When these objects are present monitor the patient during therapy and have the patient notify the operator of warming or other sensation; cease rTMS treatment in event of warming sensation) or within 30 cm of the treatment coil. (Examples include implanted electrodes/stimulators, aneurysm clips or coils, stents, bullet fragments, jewellery, and hair barrettes) \*\*This term applies to patients with a documented medical history of a decompensated health condition requiring medical treatment and/or medication, yet has not received such treatment and/or medication. Patients who use certain medications only for preventive purposes, without any proven previous health condition failure are not considered contraindicated.

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As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • DP Neuro s.r.o.

    Prague, Prague, 162 00, Czechia