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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03039829
Other study ID # IRB2015-0684
Secondary ID
Status Completed
Phase N/A
First received January 20, 2017
Last updated January 30, 2017
Start date January 2016
Est. completion date May 2016

Study information

Verified date January 2017
Source Texas A&M University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study will aim to determine whether ingesting creatine nitrate (CrN) at higher doses will differentially affect hemodynamic variables compared to a placebo.


Description:

This study will examine the short-term (7 day) characteristics of ingesting creatine nitrate (CrN) compared to placebo on Chem-15 blood safety, heart rate, blood pressure, heart rate and blood pressure reactivity and self-reported side effects.


Recruitment information / eligibility

Status Completed
Enrollment 38
Est. completion date May 2016
Est. primary completion date May 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 40 Years
Eligibility Inclusion Criteria:

- Apparently healthy

- At least 6 months immediate prior history of resistance training including bench press and leg press or squat

Exclusion Criteria:

- A history of treatment for metabolic disease (i.e., diabetes), hypertension, hypotension, thyroid disease, arrhythmias and/or cardiovascular disease

- Use of prescription medication (birth control is allowed)

- Pregnant or nursing or plan to become pregnant during the next month

- Creatine or nitrate use in the last eight weeks

- History of smoking

- History of drinking (i.e., 12 drinks per week or more)

- Use of nonsteroidal anti-inflammatory drugs (NSAIDs) including ibuprofen (Advil, Motrin, Nuprin, etc.), indomethacin (Indocin), naproxen (Aleve, Anaprox, Naprelan, Naprosyn), piroxicam (Feldene)

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Creatine nitrate, low dose
Creatine nitrate at 3.0 grams (2.0 grams creatine, 1.0 gram nitrate, 3.0 grams dextrose)
Creatine nitrate, high dose
Creatine nitrate at 6.0 grams (4.0 grams creatine, 2.0 grams nitrate)
Placebo
Placebo at 6.0 grams (6.0 grams dextrose)

Locations

Country Name City State
n/a

Sponsors (2)

Lead Sponsor Collaborator
Texas A&M University Nutrabolt

Outcome

Type Measure Description Time frame Safety issue
Primary Measuring the blood pressure response to creatine nitrate ingestion 7 days
Primary Measuring the heart rate response to creatine nitrate ingestion 7 days
Secondary Measuring a blood chemistry panel 15 response to creatine nitrate ingestion 7 days
Secondary Measuring the one Repetition Maximum (1 RM) muscle strength response to creatine nitrate ingestion 7 days
Secondary Measuring the repetitions to failure muscle endurance response to creatine nitrate ingestion 7 days
Secondary Measuring self-reported side effects of creatine nitrate ingestion 7 days
See also
  Status Clinical Trial Phase
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