Salicornia for Neurovascular Health Improve

Status Recruiting

Clinical Trial Summary

The purpose of this study is evaluate the effect and safety of the administration of a food supplement based on halophyte plant extracts versus placebo in the neurovascular healthy.

Clinical Trial Description

After being informed about the study and giving written informed consent, healthy volunteers (substudy A), patients with transient ischemic attack (TIA) or MINOR stroke (substudy B), patients with cerebral small vessel disease (substudy C) and patients who have suffered a non-disabling stroke and are going to receive carotid angioplasty and stenting (CAS) (substudy D) will be randomized in double-blind manner (participant and investigator) to take a food supplement based on halophyte plant extracts (1 g once a day) or placebo (once a day) for a treatment period of 3 months (substudy A), 11 months (substudy B), 1 year (substudy C) or 7-30 days (substudy D). Participants in substudy A will be twice as likely to be assigned to the experimental treatment as to placebo (2:1 ratio), while those in substudies B, C and D will be equally likely (1:1 ratio). ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT06076122
Study type	Interventional
Source	Fundación Pública Andaluza para la gestión de la Investigación en Sevilla
Contact
Status	Recruiting
Phase	N/A
Start date	September 15, 2022
Completion date	October 31, 2023

View Details

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