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COMPLETED

Minoxidil Response Testing in Females With Female Pattern Hair Loss

NCT02206802 · View on ClinicalTrials.gov ↗

Study Summary

The primary purpose of this study is to evaluate the clinical validity of the minoxidil response in-vitro diagnostic kit.

Interventions

  • DRUG 5% minoxidil topical foam

Study Locations (5)

Other

  • Sinclair Dermatology — East Melbourne
  • LTM Medical College & Hospital — Mumbai
  • Istituto Medico Tricologico/Studi Life Cronos — Florence

Arizona

  • Physicians Hair Institute — Tucson

Tennessee

  • Tennessee Clinical Research Center — Nashville

Trial Details

FieldValue
Enrollment Target 300 participants
Start Date 2014-07
Est. Completion 2018-10

Sponsor

Applied Biology

3 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT02206802

The ClinicalTrials.gov registry entry for NCT02206802 describes a study currently listed as completed. It is categorized as an unspecified phase, 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 300 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Applied Biology, which has 3 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 2 conditions, with Alopecia appearing as the primary indexed condition, and to 1 intervention — of which 5% minoxidil topical foam 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: NCT02206802 reports 5 study locations spanning 3 distinct geographic areas — top geographies include Other, Arizona, Tennessee. 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 NCT02206802 about?

NCT02206802 is a clinical study titled "Minoxidil Response Testing in Females With Female Pattern Hair Loss". The primary purpose of this study is to evaluate the clinical validity of the minoxidil response in-vitro diagnostic kit.

What is the current status of trial NCT02206802?

This trial is currently completed. The enrollment target is 300 participants. The study started on 2014-07. Estimated completion is 2018-10.

What conditions does trial NCT02206802 study?

This clinical trial studies the following conditions: Alopecia, Female Pattern Hair Loss. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT02206802?

The interventions under investigation include: 5% minoxidil topical foam (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT02206802?

This trial is sponsored by Applied Biology, which has 3 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT02206802 being conducted?

This trial has 5 study locations across Arizona, Tennessee. 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