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Effects of allicin pretreatment on anti-oxidation ability and delayed onset muscle soreness

NCT ID NCT07812688

NEW Sponsor: Guangxi Normal University Source: ClinicalTrials.gov ↗

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Sep 10, 2026 · Last updated Sep 10, 2026

Summary

To investigate the effects of allicin pretreatment on delayed onset muscle soreness (DOMS), muscle function, and oxidative stress following eccentric exercise

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

30 people

The number who actually took part.

Started

Apr 2024

Finished

Jun 2024

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 to 24 years

Sex

Male participants only

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Participants voluntarily agreed to join the study and signed informed consent forms. * Male participants aged between 18 and 24 years. * Physically healthy, with no history of major or congenital diseases. * Normal results in routine physical examinations, with no history of severe musculoskeletal injuries. * Physical fitness levels equivalent to those of typical university students majoring in sports. * During the entire experiment, participants must not engage in any intense physical activities other than the specified exercise protocol. Exclusion Criteria: * Participants with poor compliance or those who violate the experimental requirements. * Participants who are unwilling to cooperate and fail to complete the required data collection for the experiment. * Participants who have taken anti-inflammatory or steroid medications within the past month. * Participants who have experienced musculoskeletal injuries within the past two months.

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As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Delayed onset muscle soreness

Contacts and locations

Locations

  • Guangxi Normal University

    Guilin, China

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