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

NCT07485231 · ClinicalTrials.gov registry record · NA

Nitric Oxide (NO) and Endothelial Dysfunction in Women With PTSD

A NA study, sponsored by University of Minnesota.

Recruiting
Registry status
NA
Development phase
30
Enrollment target

NCT07485231: Recruiting NA study, sponsored by University of Minnesota.

NCT07485231 is a NA study that is actively recruiting participants, run by University of Minnesota. The registered enrollment target is 30 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT07485231, a NA study, is actively recruiting participants, sponsored by University of Minnesota.

RECRUITING
Registry status
NA
Development phase
30 participants
Enrollment target

Study Summary

This research study is conducted to better understand why women with post-traumatic stress disorder (PTSD) have higher risk of cardiovascular disease as they get older. This study looks at how trauma and PTSD affect blood vessels in young women by testing whether the dietary supplement beetroot juice might help improve the function of blood vessels in women suffering from PTSD.

Primary Outcome

Difference in FMD before and after beetroot juice administration

Interventions

  • DIETARY_SUPPLEMENT Placebo Juice
  • DIETARY_SUPPLEMENT Beetroot Juice

Trial Details

FieldValue
Enrollment Target 30 participants
Start Date 2026-02-18
Est. Completion 2028-05-01
Phase NA
University of Minnesota

966 total trials

What NCT07485231 shows while recruiting

NCT07485231 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 30 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower).

The record links to 0 conditions, and to 2 interventions - of which Placebo Juice is the first listed.

NCT07485231 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT07485231 about?

NCT07485231 is a clinical study titled "Nitric Oxide (NO) and Endothelial Dysfunction in Women With PTSD". This research study is conducted to better understand why women with post-traumatic stress disorder (PTSD) have higher risk of cardiovascular disease as they get older. This study looks at how trauma and PTSD affect blood vessels in young women by testing whether the dietary supplement beetroot juic...

What is the current status of trial NCT07485231?

This trial is currently recruiting. It is a NA study. The enrollment target is 30 participants. The study started on 2026-02-18. Estimated completion is 2028-05-01.

What interventions are being tested in trial NCT07485231?

The interventions under investigation include: Placebo Juice (DIETARY_SUPPLEMENT), Beetroot Juice (DIETARY_SUPPLEMENT).

Who is sponsoring clinical trial NCT07485231?

This trial is sponsored by University of Minnesota, which has 966 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT07485231's enrollment target sits among peer trials

30 1593rd of 2000 higher than 299 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA 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

  • NCT00977977 · 30 participants · Phase 2

    Rituximab Plus Cyclosporine in Idiopathic Membranous Nephropathy

  • NCT01459107 · 30 participants · Phase 2

    Human Upper Extremity Allotransplantation

  • NCT01666080 · 30 participants · NA

    Second or Greater Allogeneic Hematopoietic Stem Cell Transplant Using Reduced Intensity Conditioning (RIC)

  • NCT01720836 · 30 participants · Phase 1

    Study of the Immune Response of MUC1 (Mucin1) Peptide Vaccine for Non-small Cell Lung Cancer

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 NCT07485231, the US trial registry maintained by the National Library of Medicine. NCT07485231 (small enrollment · none site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.