Viewing Study NCT05644769


Ignite Creation Date: 2025-12-24 @ 10:55 PM
Ignite Modification Date: 2026-02-18 @ 2:40 AM
Study NCT ID: NCT05644769
Status: UNKNOWN
Last Update Posted: 2022-12-09
First Post: 2022-11-22
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: Chymase Angiotensin-(1-12) Axis In Hypertensive Disease
Sponsor: Trinity Hypertension & Metabolic Research Institute
Organization:

Study Overview

Official Title: The Chymase Angiotensin-(1-12) Axis in Hypertensive Disease
Status: UNKNOWN
Status Verified Date: 2022-12
Last Known Status: RECRUITING
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: Determine the presence of the human sequence of Angiotensin-(1-12) in plasma of ten untreated hypertensive subjects and after 4 week with Lisinopril 40 mg every day. Determine the blood pressure reduction with Lisinopril 40mg.
Detailed Description: Determine the presence of the human sequence of Ang-(1-12) in the plasma of ten normal male and female hypertensive patients at baseline and after 4 weeks on Lisinopril 40mg every day. Measure concentrations of Ang-(1-12) in either spot urine collections from ten male and female hypertensive patients at baseline and after 4 weeks of Lisinopril 40mg every day.

Study Oversight

Has Oversight DMC: False
Is a FDA Regulated Drug?: True
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: False
Is an FDA AA801 Violation?: