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Blood Pressure ControlNCT07844239

Direct Electrical Stimulation of Central Autonomic Network for Blood Pressure Control: a Mechanism Study

A study testing direct electrical stimulation in people with Blood Pressure Control and Hypertension, run by Xuanwu Hospital, Beijing.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
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Trial summary

The primary objective of this research is to study direct electrical stimulation of central autonomic network for blood pressure control. Read more about this study

Who is it for?
Ages 18 to 60 years
Conditions the study is for
Blood Pressure Control, Hypertension
What is being tested?
direct electrical stimulation
Could I receive a placebo?
No, everyone receives an active treatment
How many people
20 participants
Where
No sites listed yet
Study dates
1 Sep 2026to 31 Dec 2026
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 60 years
  • All sexes
  • No healthy volunteers
  • Adult

Who may be able to join

  • Aged 18-60 years, with no gender restrictions.
  • Free from severe systemic diseases.
  • Patients who have undergone stereoelectroencephalography electrode implantation.
  • Patients who have been informed of potential risks, consented to participate in this study, and signed the informed consent form.
  • Daytime clinic blood pressure fluctuates within the following range: 90 mmHg < systolic blood pressure < 140 mmHg; 60 mmHg < diastolic blood pressure < 90 mmHg.

Who cannot join

  • Patients with scalp electrode hematoma or sub-electrode effusion after intracranial electrode implantation, who are unable to receive electrical stimulation.
  • Patients with intracranial structural lesions (e.g., encephalomalacia foci, vascular malformations, space-occupying lesions, etc.).
  • Pregnant women.
  • Patients who are unable to cooperate due to mental disorders or other causes.
  • Patients who have participated in other clinical trials within the past 3 months.
  • Patients who apply to withdraw from this clinical trial for any reason.
Show all 9Show fewer
  • Patients with cardiac or pulmonary insufficiency.
  • Patients with white coat effect are excluded.
  • Patients with low cerebrovascular risk assessed by cranial magnetic resonance imaging (MRI).

Trial locations and contacts

No sites are listed yet. Contact the study team or a site near you to ask about taking part.

About this study

The primary objective of this research is to study direct electrical stimulation of central autonomic network for blood pressure control.

Read the detailed description

This project aims to include 20 participants, and evaluate the direct electrical stimulation of central autonomic network for blood pressure control through A pilot, prospective clinical trial. It is expected to explore potential blood pressure regulation-related targets in the central autonomic neural network and provide a neuromodulation approach for the treatment of blood pressure disorders, including refractory hypertension and neurogenic orthostatic hypotension.

Being tested
direct electrical stimulation
Keywords
blood pressure control, central autonomic neural network, direct electrical stimulation, hypertension
Medical subject headings
Hypertension

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • direct electrical stimulationOther

    The intervention consists of direct electrical stimulation delivered at three distinct frequencies (10 Hz, 50 Hz, and 120 Hz). A double-blind design will be employed to randomly assign one of these frequencies for a 30-second direct electrical stimulation session in each patient.

Study groups in NCT07844239
Study groupRoleWhat they receive
Direct electrical stimulationExperimentalPatients with hypertension and drug-resistant focal epilepsy who underwent intracranial monitoring via stereotactically implanted depth electrodes (SEEG) are assigned to Direct electrical stimulation for 30 sec per mission.
Receives: Other: direct electrical stimulation

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. blood pressure

    Blood Pressure is defined as the blood pressure measurement obtained 30 minutes after the completion of direct electrical stimulation.

    Measured: up to 4 hours

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted28 Sep 2026
  2. Study start1 Sep 2026 (estimated)
  3. Primary completion31 Dec 2026 (estimated)
  4. Study completion31 Dec 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
20 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07844239
Sponsor's protocol ID
2025-330-002
Status last verified
Dec 2025
First submitted
22 Sep 2026
Last updated
28 Sep 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing direct electrical stimulation in people with Blood Pressure Control and Hypertension, run by Xuanwu Hospital, Beijing.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 9 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: opening soon, as of the sponsor's last update on 28 Sep 2026. Status can change between updates, so confirm with the study contact before making plans.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Liankun Ren, MD (+86 13681576621, renlk2022@outlook.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

blood pressure (time frame: up to 4 hours). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 28 Sep 2026; AzTrials last refreshed its copy on 7 Nov 2026.

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