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COMPLETED NA

Moringa Powder Acceptability Trial Among Healthy Adults

NCT05861076 · View on ClinicalTrials.gov ↗

Study Summary

The study is a randomized acceptability trial involving the provision of three different doses of Moringa powder to be consumed daily by study participants.

Interventions

  • OTHER Moringa Powder - Low Dose
  • OTHER Moringa Powder - Medium Dose
  • OTHER Moringa Powder - High Dose

Study Locations (1)

California

  • University of California — Berkeley

Trial Details

FieldValue
Enrollment Target 52 participants
Start Date 2023-01-03
Est. Completion 2023-05-30
Phase NA

Sponsor

University of California, Berkeley

60 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT05861076

The ClinicalTrials.gov registry entry for NCT05861076 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 52 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of California, Berkeley, which has 60 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 3 conditions, with Acceptability appearing as the primary indexed condition, and to 3 interventions — of which Moringa Powder - Low Dose 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: NCT05861076 reports 1 study location spanning 1 distinct geographic area — top geographies include California. 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 NCT05861076 about?

NCT05861076 is a clinical study titled "Moringa Powder Acceptability Trial Among Healthy Adults". The study is a randomized acceptability trial involving the provision of three different doses of Moringa powder to be consumed daily by study participants.

What is the current status of trial NCT05861076?

This trial is currently completed. It is a NA study. The enrollment target is 52 participants. The study started on 2023-01-03. Estimated completion is 2023-05-30.

What conditions does trial NCT05861076 study?

This clinical trial studies the following conditions: Acceptability, Side Effect, Consumption. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT05861076?

The interventions under investigation include: Moringa Powder - Low Dose (OTHER), Moringa Powder - Medium Dose (OTHER), Moringa Powder - High Dose (OTHER). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT05861076?

This trial is sponsored by University of California, Berkeley, which has 60 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT05861076 being conducted?

This trial has 1 study location across California. 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