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COMPLETED Phase 3

A Study to Evaluate the Therapeutic Equivalence of Generic Permethrin Cream 5% to Elimite® in the Treatment of Scabies

NCT02572986 · View on ClinicalTrials.gov ↗

Study Summary

Scabies is an infestation of the skin by the human itch mite (Sarcoptes scabiei). Diagnosis of scabies is made based on clinical symptoms, such as nocturnal itching, and appearance and distribution of the rash. Definitive diagnosis includes the microscopic identification of the mite, mite eggs, or mite fecal matter in the skin. Topical permethrin is considered the drug of choice for the treatment of scabies. It is a synthetic pyrethroid that is safe for use in adults and children 2 months and older. This study will evaluate the therapeutic equivalence of a generic permethrin cream 5% to Elimite® in the Treatment of Scabies.

Conditions Studied

Interventions

  • DRUG Permethrin

Study Locations (13)

Florida

  • Solutions Through Advanced Research — Jacksonville
  • San Marcus Research Clinic, Incorporation — Miami
  • L & C Professional Medical Research Institute — Miami
  • Vista Health Research, LLC — Miami

California

  • Sun Rise Clinical Research, Inc — Bell Gardens
  • Havana Research Institute — Pasadena

Other

  • Clinica Dermatologica — San Salvador
  • Clinica Dermatologica y Cirugia de Piel — Santa Tecla, La Libertad

Arizona

  • Omni Dermatology — Phoenix

Pennsylvania

  • Derm Dx Center for Dermatology — Hazleton

Texas

  • Sun Research Institute — San Antonio

Washington

  • Zain Research, LLC — Richland

PanamaCity

  • Clinica Dermatologica Dra. Yariela Grajales — Panama City

Trial Details

FieldValue
Enrollment Target 250 participants
Start Date 2015-09
Est. Completion 2016-08
Phase Phase 3

Sponsor

Dr. Reddy's Laboratories Limited

14 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT02572986

The ClinicalTrials.gov registry entry for NCT02572986 describes a study currently listed as completed. It is categorized as Phase 3, 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 250 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Dr. Reddy's Laboratories Limited, which has 14 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Scabies appearing as the primary indexed condition, and to 1 intervention — of which Permethrin 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: NCT02572986 reports 13 study locations spanning 8 distinct geographic areas — top geographies include Florida, California, Other. 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 NCT02572986 about?

NCT02572986 is a clinical study titled "A Study to Evaluate the Therapeutic Equivalence of Generic Permethrin Cream 5% to Elimite® in the Treatment of Scabies". Scabies is an infestation of the skin by the human itch mite (Sarcoptes scabiei). Diagnosis of scabies is made based on clinical symptoms, such as nocturnal itching, and appearance and distribution of the rash. Definitive diagnosis includes the microscopic identification of the mite, mite eggs, or m...

What is the current status of trial NCT02572986?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 250 participants. The study started on 2015-09. Estimated completion is 2016-08.

What conditions does trial NCT02572986 study?

This clinical trial studies the following conditions: Scabies. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT02572986?

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

Who is sponsoring clinical trial NCT02572986?

This trial is sponsored by Dr. Reddy's Laboratories Limited, which has 14 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT02572986 being conducted?

This trial has 13 study locations across Arizona, California, Florida, Pennsylvania, Texas. 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