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Randomized Study to Compare the Bioavailability of Two Fluticasone Propionate 0.005% Topical Ointments

NCT00803218 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 56

Last updated 2021-10-15

No results posted yet for this study

Summary

The purpose of this study was to compare the relative vasoconstrictive effects of test and reference topical Fluticasone Propionate 0.005% Ointments in healthy, female subjects.

Conditions

  • Healthy

Interventions

DRUG

Fluticasone Propionate 0.005% Ointment-Reference Product

Small amount applied and evaluated over the course of one day

DRUG

Fluticasone Propionate 0.005% Ointment-Test product

Small amount applied and evaluated over the course of one day

Sponsors & Collaborators

  • Padagis LLC

    lead INDUSTRY

Eligibility

Min Age
18 Years
Max Age
50 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2002-11-30
Primary Completion
2002-11-30
Completion
2002-11-30

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00803218 on ClinicalTrials.gov