Grape seed supplement shows promise in lowering jaundice bilirubin

NCT ID NCT07575789

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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 Results may not be published yet.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
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Status unknown
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First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study tested whether taking grape seed powder along with vitamin C could lower bilirubin levels in people with jaundice caused by liver issues. Twenty-four adults with high bilirubin and other liver markers took the supplement or standard care. Results showed a significant drop in bilirubin for the supplement group, suggesting it may help ease jaundice symptoms.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
grape seed powder and vitamin C supplement
What this could lead to
If it works, this could offer a simple dietary supplement to help reduce jaundice symptoms by lowering bilirubin levels.
What could go wrong
This is a very small, completed study with only 24 participants. The results may not apply to everyone, and the supplement is not a treatment for the underlying liver disease.

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

24 people

The number who actually took part.

Started

Mar 2023

Finished

Apr 2023

Lead sponsor

A research network

The lead sponsor is a research network or cooperative group.

Who can take part

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

Ages

20 to 40 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

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: * Both men and women * Participants between the ages of 20-40 years will be included * Patients having signs and symptoms of acquired hepatic jaundice * Patients having high serum bilirubin, albumin, ALT, AST, ALP levels * The patient having ALT level more than 10-50 U/L were included * The participants having AST level above than 0-40 IU/L were included in this study * Patients having ALP level more than 30 - 130 U/L were included in this research study * Patients having level of bilirubin above than 0 - 21 μmol/L were included in this investigation * Participants having the range of albumin more than 30-50 g/L were included in this research * Participants those were underweighted were included Exclusion Criteria: * Patients who already taking any supplement or medication * Participants taking any anti-inflammatory medications * People who were suffering from any other disease * Patients who have any known allergies * Non willing patients * Lactating women * Pregnant women * Smokers

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Conditions

The condition(s) this trial relates to.

Jaundice

As listed by the trial registrant

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

Contacts and locations

Locations

  • University of Lahore

    Lahore, Punjab Province, Pakistan

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