CClinicalTrials.gg
CompletedNCT00551434Updated Oct 31, 2007

Effect of Creatine and L-Arginine on Endothelial Function

An interventional study of Creatine and L-arginine and creatine in Coronary Artery Disease, sponsored by Boston University. Completed. Open to participants aged 18 Years to 80 Years. Per ClinicalTrials.gov, last updated 2007-10-31.

Sponsored by Boston University · Not applicable, Interventional, and Basic science

Phase
Not applicable
Study type
Interventional
Enrollment
119
Allocation
Randomized
Ages
18 Years to 80 Years
Sex
All
01

Study summary

The study is a double blind 2x2 factorial study. Patients with coronary disease will be randomly be assigned to L-arginine (9 g/day), creatine 21 g/d, both, or neither dietary supplement. The function of the endothelium will be tested using ultrasound before and after each treatment. These studies will help us understand why the endothelium is abnormal in patients with coronary artery disease and how L-arginine is acting on endothelial function.

02

Conditions studied

03

In context

Coronary Artery Disease

5,598 studies on the registry are indexed under Coronary Artery Disease; 957 are open to participants now.

This study's enrollment of 119 is close to the median of 124 across 3,436 interventional studies indexed under Coronary Artery Disease.

Browse Coronary Artery Disease studies →

Lead sponsor

Boston University is the lead sponsor of 266 studies on the registry; 37 are open to participants now.

Of its 30 completed or terminated interventional studies of FDA-regulated products, 24 (80%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 80 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Coronary artery disease

Exclusion criteria

Exclusion Criteria:

  • Pregnancy
  • Creatine use within one month of study
  • L-arginine use within one month of study
  • Change in dose or initiation of lipid lowering therapy, aspirin therapy, or angiotensin converting enzyme therapy within one month of study
05

Study design

Phase
Not applicable
Primary purpose
Basic science
Allocation
Randomized
Intervention model
Factorial assignment
Masking
Triple (Participant, Investigator, Outcomes assessor)
Enrollment
119 participants (actual)

Study arms

  • Experimental
    1

    Dietary Supplement: Creatine

  • Experimental
    2

    Dietary Supplement: l-arginine

  • Experimental
    3

    Dietary Supplement: L-arginine and creatine

  • Placebo comparator
    4

    Dietary Supplement: placebo, double

Interventions

  • Dietary supplementCreatine

    Creatine 21 g daily

  • Dietary supplementL-arginine and creatine

    L-arginine

  • Dietary supplementl-arginine

    l-arginine 9 g daily

  • Dietary supplementplacebo, double

    placebo

06

What researchers measure

Primary outcomes

  1. Brachial artery flow-mediated dilation

    Time frame: 5 days

Secondary outcomes

  1. serum arginine, creatine, creatinine, homocysteine

    Time frame: 5 days

07

Study locations

No study locations are listed for this record.

08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 31, 2007, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT00551434
Lead sponsor
Boston University
First posted
Oct 31, 2007
Start date
Aug 2002
Completion
Dec 2005
Last update
Oct 31, 2007

Study contacts

Joseph A Vita, MD
principal investigator · Boston Medical Center

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Oct 2007. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion