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Nitrate Supplementation and Exercise Tolerance in Patients With Type 2 Diabetes

NCT02804932 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 54

Last updated 2024-05-28

Study results available
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Summary

The purpose of this study is to use a randomized, double-blind, placebo controlled study design to comprehensively investigate the impact of 8-weeks of dietary nitrate supplementation on skeletal muscle blood flow, mitochondrial function, and exercise capacity in patients with type 2 diabetes (T2D).

Conditions

Interventions

DIETARY_SUPPLEMENT

Super Beets

Nitrate rich beetroot powder (10g/day) for 8 weeks

OTHER

Super Beets Placebo

Nitrate deficient beetroot powder (10g/day) for 8 weeks

Sponsors & Collaborators

Principal Investigators

  • Darren P Casey, PhD · University of Iowa

Study Design

Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
40 Years
Max Age
77 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2016-08-15
Primary Completion
2019-12-20
Completion
2019-12-20

Countries

  • United States

Study Locations

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Entities

Diseases
Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02804932 on ClinicalTrials.gov