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NCT05877417 · ClinicalTrials.gov registry record · NA

Blood Flow Restriction and Creatine Supplementation in Women

A NA study, sponsored by University of Central Florida.

Completed
Registry status
NA
Development phase
68
Enrollment target

NCT05877417: Completed NA study, sponsored by University of Central Florida.

NCT05877417 is a NA study that has completed, run by University of Central Florida. The registered enrollment target is 68 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (95% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT05877417, a NA study, has completed, sponsored by University of Central Florida.

COMPLETED
Registry status
NA
Development phase
68 participants
Enrollment target

Study Summary

This research is examining the changes in muscle size, muscle function, body composition, strength, and blood vessel health. Specifically, the changes in these variables over the course of 8 weeks of training with or without blood flow restriction (BFR) and the supplementation of creatine or placebo (dextrose, a sugar in the form of a powder which is the standard placebo). Creatine monohydrate (Cr) is the most popular supplement for athletes and benefits all populations, however women are still very hesitant to take it due to the misconception of weight gain. This study will look to measure those muscle and body changes with exercise.

Primary Outcome

isokinetic dynanometer

Interventions

  • OTHER Exercise
  • DIETARY_SUPPLEMENT Creatine Monohydrate
  • DEVICE Blood Flow Restriction

Trial Details

FieldValue
Enrollment Target 68 participants
Start Date 2023-05-17
Est. Completion 2024-03-01
Phase NA
University of Central Florida

91 total trials

What the finished NCT05877417 record still lists

NCT05877417 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 68 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (95% lower).

The record links to 0 conditions, and to 3 interventions - of which Exercise is the first listed.

NCT05877417 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT05877417 about?

NCT05877417 is a clinical study titled "Blood Flow Restriction and Creatine Supplementation in Women". This research is examining the changes in muscle size, muscle function, body composition, strength, and blood vessel health. Specifically, the changes in these variables over the course of 8 weeks of training with or without blood flow restriction (BFR) and the supplementation of creatine or placebo...

What is the current status of trial NCT05877417?

This trial is currently completed. It is a NA study. The enrollment target is 68 participants. The study started on 2023-05-17. Estimated completion is 2024-03-01.

What interventions are being tested in trial NCT05877417?

The interventions under investigation include: Exercise (OTHER), Creatine Monohydrate (DIETARY_SUPPLEMENT), Blood Flow Restriction (DEVICE).

Who is sponsoring clinical trial NCT05877417?

This trial is sponsored by University of Central Florida, which has 91 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT05877417's enrollment target sits among peer trials

68 1133rd of 2000 higher than 862 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT05877417, the US trial registry maintained by the National Library of Medicine. NCT05877417 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.