Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT06094816 · ClinicalTrials.gov registry record · Phase 4

Forebrain Electroneutral Transporters in Salt-sensitive Hypertension: an MRI Study

A Phase 4 study of Salt-Sensitivity of Blood Pressure, sponsored by University of Delaware.

Recruiting
Registry status
Phase 4
Development phase
120
Enrollment target
1
Study location

NCT06094816: Recruiting Phase 4 study of Salt-Sensitivity of Blood Pressure, sponsored by University of Delaware.

NCT06094816 is a Phase 4 study of Salt-Sensitivity of Blood Pressure that is actively recruiting participants, run by University of Delaware. The registered enrollment target is 120 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (77% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT06094816, a Phase 4 study of Salt-Sensitivity of Blood Pressure, is actively recruiting participants, sponsored by University of Delaware.

RECRUITING
Registry status
Phase 4
Development phase
120 participants
Enrollment target
1
Study location

Study Summary

The overall objective of this project is to identify the key salt-sensing regions of the brain and determine the underlying mechanism of sodium sensing. The investigators will assess how the brain responds to an acute increase of salt in the blood using MRI. This will be done during a 30-minute infusion of a saline solution containing 3% salt. One trial will be conducted with a salt sensing channel blocker and one trial without the salt sensing channel blocker. This will help to assess the role of a specific salt sensing channel in the brain. Salt sensitivity of BP will be assessed using 7-day dietary feeding where participants will be given food to consume for 7-days. Comparisons will be made between salt resistant (no change in blood pressure going from low to high salt diets) and salt sensitive adults (a change in blood pressure going from low to high salt diets). The investigators think the changes in MRI will be greater in salt sensitive compared to salt resistant subjects.

Primary Outcome

Intensity of sodium sensing regions of the brain

Interventions

  • DRUG Furosemide (Diuretic)
  • OTHER Hypertonic Saline Infusion

Study Locations (1)

Delaware

  • University of Delaware - Newark

Trial Details

FieldValue
Enrollment Target 120 participants
Start Date 2024-03-05
Est. Completion 2028-07
Phase Phase 4
University of Delaware

106 total trials

What NCT06094816 shows while recruiting

NCT06094816 is an interventional study that assigns participants to a tested intervention. The registered 120 participants enrollment target is mid-sized for trials with a published cap, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (77% lower).

The record links to 1 condition, with Salt-Sensitivity of Blood Pressure appearing as the primary indexed condition, and to 2 interventions - of which Furosemide (Diuretic) is the first listed.

NCT06094816 reports a single indexed study location in Delaware.

Frequently Asked Questions

What is clinical trial NCT06094816 about?

NCT06094816 is a clinical study titled "Forebrain Electroneutral Transporters in Salt-sensitive Hypertension: an MRI Study". The overall objective of this project is to identify the key salt-sensing regions of the brain and determine the underlying mechanism of sodium sensing. The investigators will assess how the brain responds to an acute increase of salt in the blood using MRI. This will be done during a 30-minute infu...

What is the current status of trial NCT06094816?

This trial is currently recruiting. It is a Phase 4 study. The enrollment target is 120 participants. The study started on 2024-03-05. Estimated completion is 2028-07.

What conditions does trial NCT06094816 study?

This clinical trial studies the following conditions: Salt-Sensitivity of Blood Pressure.

What interventions are being tested in trial NCT06094816?

The interventions under investigation include: Furosemide (Diuretic) (DRUG), Hypertonic Saline Infusion (OTHER).

Who is sponsoring clinical trial NCT06094816?

This trial is sponsored by University of Delaware, which has 106 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06094816 being conducted?

This trial has 1 study location across Delaware. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Salt-Sensitivity of Blood Pressure

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT06094816's enrollment target sits among peer trials

120 673rd of 2000 higher than 1,290 of 2,000 other Phase 4 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 4 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT01174108 · 120 participants · Phase 2

    Allogeneic Hematopoietic Stem Cell Transplantation for Severe Aplastic Anemia and Other Bone Marrow Failure Syndromes Using G-CSF Mobilized CD34+ Selected Hematopoietic Precursor Cells Co-Infused With a Reduced Dose of Non-Mobilized Donor T-cells

  • NCT01627301 · 120 participants · NA

    Sympathetic Overactivity in Post-traumatic Stress Disorder

  • NCT02025023 · 120 participants · Phase 3

    Local 5-Fluorouracil Injection for the Treatment of Chalazia: A Prospective, Comparative Study

  • NCT02128906 · 120 participants · Phase 2

    Radiotherapy With Cisplatin vs. Docetaxel-cetuximab in HNSCC: ERCC1 Biomarker Enrichment and Interaction Design

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT06094816, the US trial registry maintained by the National Library of Medicine. NCT06094816 (mid enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.