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COMPLETED NA

The Effect of Blood Flow Restriction With and Without Arginine on Physical Performance and Growth Hormone

NCT04079010 · View on ClinicalTrials.gov ↗

Study Summary

The current study will investigate the effects of Blood Flow Restriction (BFR) training and L-arginine supplementation on recreationally trained female participants. In particular, it will compare performance outcomes and blood markers among two intervention groups (BFR and BFR+Arg) and a control group (CON).

Interventions

  • DIETARY_SUPPLEMENT Arginine
  • PROCEDURE BFR
  • DIETARY_SUPPLEMENT Placebo Pill

Study Locations (1)

Texas

  • University of Mary Hardin-Baylor — Belton

Trial Details

FieldValue
Enrollment Target 30 participants
Start Date 2019-09-04
Est. Completion 2019-11-25
Phase NA

Sponsor

University of Mary Hardin-Baylor

3 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT04079010

The ClinicalTrials.gov registry entry for NCT04079010 describes a study currently listed as completed. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 30 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Mary Hardin-Baylor, which has 3 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 4 conditions, with Blood Flow Restriction appearing as the primary indexed condition, and to 3 interventions — of which Arginine is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT04079010 reports 1 study location spanning 1 distinct geographic area — top geographies include Texas. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT04079010 about?

NCT04079010 is a clinical study titled "The Effect of Blood Flow Restriction With and Without Arginine on Physical Performance and Growth Hormone". The current study will investigate the effects of Blood Flow Restriction (BFR) training and L-arginine supplementation on recreationally trained female participants. In particular, it will compare performance outcomes and blood markers among two intervention groups (BFR and BFR+Arg) and a control gr...

What is the current status of trial NCT04079010?

This trial is currently completed. It is a NA study. The enrollment target is 30 participants. The study started on 2019-09-04. Estimated completion is 2019-11-25.

What conditions does trial NCT04079010 study?

This clinical trial studies the following conditions: Blood Flow Restriction, Growth Hormone, Strength Outcomes, Arginine. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT04079010?

The interventions under investigation include: Arginine (DIETARY_SUPPLEMENT), BFR (PROCEDURE), Placebo Pill (DIETARY_SUPPLEMENT). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT04079010?

This trial is sponsored by University of Mary Hardin-Baylor, which has 3 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT04079010 being conducted?

This trial has 1 study location across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial