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Herbal extract shows promise in calming schizophrenia

NCT ID NCT07575516

Symptom relief Sponsor: Hasanuddin University Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study tested whether adding ashwagandha extract to standard schizophrenia medication (risperidone) could reduce inflammation and improve symptoms. 80 male patients took part. Researchers measured changes in a blood marker for inflammation (IL-1β) and used a standard symptom scale (PANSS) to track progress. The goal was to see if ashwagandha could be a helpful add-on therapy.

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

Phase 2

Tests whether the treatment actually works, and watches for side effects, in a larger group.

Participants

80 people

The number who actually took part.

Started

Oct 2025

Finished

Jan 2026

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

20 to 45 years

Sex

Male participants only

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: * Male patients diagnosed with schizophrenia based on ICD-10/PPDGJ III criteria * Aged 20-45 years * Duration of illness ≤ 5 years * Patients who have passed the acute phase (Positive and Negative Syndrome Scale-Excited Component (PANSS-EC) \< 15) * Receiving risperidone 4 mg/day * Willing to participate and provide written informed consent Exclusion Criteria: * Presence of organic comorbid diseases * History of substance abuse (NAPZA) within the last 1 year, except caffeine and nicotine * Use of anti-inflammatory drugs, antibiotics, or antioxidant agents * Intellectual disability (mental retardation)

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Conditions

The condition(s) this trial relates to.

Inflammation Neuroinflammatory Diseases neuronitis schizophrenia

As listed by the trial registrant

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

Neuroinflammation Schizophrenia patients

Contacts and locations

Locations

  • South Sulawesi Mental Hospital (RSKD Dadi)

    Makassar, South Sulawesi, 90245, Indonesia

More trials for these conditions

Other studies related to the condition(s) this trial covers.