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NCT03643783 · ClinicalTrials.gov registry record

Impact of Plasma Soluble Prorenin Receptor in Obese and Type 2 Diabetic Patients

A clinical trial, sponsored by Tulane University.

Completed
Registry status
10
Enrollment target

NCT03643783 is a clinical trial that has completed, run by Tulane University. The registered enrollment target is 10 participants.

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The verdict

NCT03643783 has completed, sponsored by Tulane University.

COMPLETED
Registry status
10 participants
Enrollment target

Study Summary

Obesity increases the risk for type 2 diabetes mellitus, high blood pressure, and mortality. Obesity is a major health problem in the United States, especially in the Deep South regions. Obesity increases the risk for T2DM, the occurrence of hypertension, and mortality; but the efficacy of long-term weight loss medications has been disappointing. There are three options available for patients who want to lose weight: lifestyle modification, pills, or weight loss by bariatric surgery. When we compare the three options available, bariatric surgery is the most effective method to lose weight at present. Bariatric surgery allows patients lose the most weight, be able to sustain the weight reduction over time and, more importantly, diabetes mellitus and other cardiovascular risk factors significantly improve. Understanding the link among obesitydiabetes-hypertension is crucial in order to develop new therapeutic targets to decrease CVD morbidity and mortality. There is less prevalence of coronary artery disease (CAD) in premenopausal women than in men, but, once initiated, the morbidity and mortality due to CAD in women is worse than in men, thus highlighting this sex difference in CVD. Indeed, women with diabetes exhibit a higher risk of myocardial infarction and stroke mortality than men, compared to people without diabetes. In obese subjects, there is inappropriate activation of the systemic and adipose renin-angiotensin system. The prorenin receptor is a molecule expressed in various tissues including fat tissue and part of it, the soluble prorenin receptor, can be secreted into the blood. The prorenin receptor is part of a very important system that regulates blood pressure and fat in our body, the renin-angiotensin system. In this prospective observational human pilot study, we will determine whether the adipose tissue is the major supplier of soluble prorenin receptor levels in the plasma of obese patients and the relationship between blood soluble prorenin recept

Trial Details

FieldValue
Enrollment Target 10 participants
Start Date 2018-09-11
Est. Completion 2019-03-31

Sponsor

Tulane University

73 total trials

What the Registry Record Tells You About NCT03643783

The ClinicalTrials.gov registry entry for NCT03643783 describes a study currently listed as completed, categorized as an unspecified phase. The registered enrollment target is 10 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Tulane University, which has 73 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 0 interventions.

NCT03643783 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT03643783 about?

NCT03643783 is a clinical study titled "Impact of Plasma Soluble Prorenin Receptor in Obese and Type 2 Diabetic Patients". Obesity increases the risk for type 2 diabetes mellitus, high blood pressure, and mortality. Obesity is a major health problem in the United States, especially in the Deep South regions. Obesity increases the risk for T2DM, the occurrence of hypertension, and mortality; but the efficacy of long-term...

What is the current status of trial NCT03643783?

This trial is currently completed. The enrollment target is 10 participants. The study started on 2018-09-11. Estimated completion is 2019-03-31.

Who is sponsoring clinical trial NCT03643783?

This trial is sponsored by Tulane University, which has 73 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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