Hypertension Trial, Recruiting NCT06980961 Sponsor: Science Valley Research Institute Condition: Hypertension
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Hypertension Trial, Recruiting

NCT06980961
Recruiting Not Applicable

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • Women and men between 18 and 89 years old who have a skin condition called stasis dermatitis, caused by high blood pressure in the veins (venous hypertension)
  • People who agree to the terms of the study and sign a consent form
  • People who are able to attend all required appointments for treatment and follow-up visits
  • People who agree to avoid becoming pregnant during the study
  • People who have already had treatment for varicose veins in the legs (using any available method) related to their venous condition

Who may not be able to join:

  • People with a venous disease classification of CEAP 2 to 6, limited mobility, and no stasis dermatitis (confirm with trial site)
  • People who have reduced blood flow to the limbs due to artery problems (peripheral arterial disease)
  • People with a known allergy to any of the medications being used in this study
  • People who have other types of skin conditions affecting the lower legs, such as allergic eczema
  • People who have certain other health conditions, including diabetes, heart failure, breathing problems, high blood pressure, thyroid disorders, asthma, or migraines — or who are pregnant, breastfeeding, have pulmonary hypertension, have had deep vein thrombosis (blood clots in the veins), have a family history of blood clots, or have a known tendency for the blood to clot too easily
  • People who do not agree to any of the study terms

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 19 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: Eduardo Ramacciotti, MD, Ph.D, livre docente, Science Valley Research Institute

Phone: +5511950212099

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Not Applicable
Sponsor
Science Valley Research Institute
Registry
ClinicalTrials.gov
Start date
20 May 2025
Est. completion
1 October 2026

Where this trial is recruiting

🇧🇷 Brazil

Primary endpoints

Colorimetry

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 19 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov