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NCT01407172 · ClinicalTrials.gov registry record

Hydrogen Sulfide and Peripheral Arterial Disease

A clinical trial, sponsored by Louisiana State University Health Sciences Center Shreveport.

Completed
Registry status
252
Enrollment target

NCT01407172: Completed study, sponsored by Louisiana State University Health Sciences Center Shreveport.

NCT01407172 is a clinical trial that has completed, run by Louisiana State University Health Sciences Center Shreveport. The registered enrollment target is 252 participants. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01407172 has completed, sponsored by Louisiana State University Health Sciences Center Shreveport.

COMPLETED
Registry status
252 participants
Enrollment target

Study Summary

This will be an observational study comparing the plasma levels of free hydrogen sulfide in patients with and without peripheral arterial disease using a novel recently published method of measuring hydrogen sulfide. The investigators will also see if there is any difference in these levels between symptomatic and asymptomatic patients. Will examine the relationship of these levels to known clinical risk factors as well as plasma nitrite and nitric oxide levels. In doing the above the investigators hope to explore the utility of free hydrogen sulfide as a biomarker for peripheral arterial disease. Atherosclerotic peripheral arterial disease (PAD) of the lower extremities represents a significant and growing cause of morbidity and mortality. The PARTNERS study of screening ABIs in a primary care population of nearly 7000 individuals demonstrated a remarkable 29% incidence of ABI \<0.9, which is the commonly accepted level of abnormal ABI diagnostic of PAD. Also of note in these patients with a new diagnosis of PAD the incidence of asymptomatic PAD was a striking 48%. The availability of a biomarker will greatly enhance the care of these patient and hopefully reduce morbidity and mortality. The investigators believe that hydrogen sulfide (H2S), an endogenously produced gasotransmitter, holds promise as a clinically useful biomarker for PAD and may also provide a possible explanation for the paradox of asymptomatic PAD in patients with ABIs less than 0.9. To date, research regarding H2S has demonstrated that it participates in a myriad of physiological functions including vasodilatation, anti-apoptotic effects, modulation of mitochondrial respiration, and changes in vascular remodeling.

Primary Outcome

Will be evaluating plasma free hydrogen sulfide levels in the three cohorts of patients.

Trial Details

FieldValue
Enrollment Target 252 participants
Start Date 2011-08
Est. Completion 2012-06

What the finished NCT01407172 record still lists

NCT01407172 is an observational study that tracks outcomes without assigning an intervention. The registered 252 participants enrollment target is mid-sized for trials with a published cap.

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

NCT01407172 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01407172 about?

NCT01407172 is a clinical study titled "Hydrogen Sulfide and Peripheral Arterial Disease". This will be an observational study comparing the plasma levels of free hydrogen sulfide in patients with and without peripheral arterial disease using a novel recently published method of measuring hydrogen sulfide. The investigators will also see if there is any difference in these levels between ...

What is the current status of trial NCT01407172?

This trial is currently completed. The enrollment target is 252 participants. The study started on 2011-08. Estimated completion is 2012-06.

Who is sponsoring clinical trial NCT01407172?

This trial is sponsored by Louisiana State University Health Sciences Center Shreveport, which has 40 total clinical trials registered on ClinicalTrials.gov.

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Source: ClinicalTrials.gov NCT01407172, the US trial registry maintained by the National Library of Medicine. NCT01407172 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.