Clinical Trials Directory

Trials / Completed

CompletedNCT02147639

Effects of Sodium Nitrate on Blood Flow in Becker Muscular Dystrophy

Status
Completed
Phase
Phase 2 / Phase 3
Study type
Interventional
Enrollment
19 (actual)
Sponsor
Cedars-Sinai Medical Center · Academic / Other
Sex
Male
Age
15 Years – 45 Years
Healthy volunteers
Not accepted

Summary

This study is intended to build on a growing body of literature showing a blood flow abnormality in patients with Becker muscular dystrophy. The investigators' laboratory recently showed that this blood flow abnormality could be corrected by a single oral dose of the drug Tadalafil (also known as Cialis). The investigators now wish to replicate these exciting results using a common nitric oxide donor (sodium nitrate).

Detailed description

There are 2 phases to this research project: (1) an initial baseline study to confirm the blood flow abnormality in Becker muscular dystrophy, and (2) a subsequent brief treatment trial. There are also 3 optional study protocols: (A) dose-escalation trial, (B) placebo trial, and (C) increased exercise intensity trial. The baseline study involves an intake history, physical examination, and phlebotomy for blood chemistries and DNA followed by non-invasive forearm blood flow studies (Near Infrared Spectroscopy, Doppler Ultrasound) before and after a brief bout of handgrip exercise (approximately 3-5 hours to complete). Blood flow studies will be performed with the subject's lower body enclosed in an airtight chamber. Blood flow and oxygen delivery to the forearm muscles will be measured before and during application of lower body negative pressure at rest and during handgrip exercise. Lower body negative pressure simulates the blood flow changes that normally occur when a person sits up after lying down. The results of the baseline study will determine which patients meet preset eligibility criteria to participate in the medication phase of the study. These criteria include (1) normal kidney and liver function tests and normal BNP levels (the latter to exclude heart failure), and (2) abnormal blood flow responses to handgrip exercise. Eligible patients will be asked to repeat the above laboratory procedures on a subsequent study day after receiving a single dose of sodium nitrate. Eligible patients will also be offered the option to repeat the above laboratory procedures on three subsequent study visits, where upon: (A) the dose of sodium nitrate is increased, (B) a placebo is ingested, and/or (C) the level of exercise in increased. The investigators plan to enroll 20 adult men with Becker muscular dystrophy.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTSodium Nitrate
DIETARY_SUPPLEMENTSodium Nitrate - double dose
DIETARY_SUPPLEMENTPlacebo
PROCEDUREIncreased exercise intensity

Timeline

Start date
2013-10-01
Primary completion
2014-05-01
Completion
2014-05-01
First posted
2014-05-28
Last updated
2020-01-14

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT02147639. Inclusion in this directory is not an endorsement.