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Human Breast Tissue Bioavailability of Topically Applied Limonene

NCT01459172 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 103

Last updated 2016-04-21

No results posted yet for this study

Summary

The overall objective of this project is to determine the safety and breast tissue bioavailability of limonene following massage application of limonene containing massage oil to the breast.

Conditions

Interventions

OTHER

limonene containing massage oil

daily massage application to the breast for 4 weeks

Sponsors & Collaborators

  • United States Department of Defense

    collaborator FED

  • University of Arizona

    lead OTHER

Principal Investigators

  • Sherry Chow, Ph.D. · The University of Arizona

Study Design

Allocation
NA
Purpose
PREVENTION
Masking
NONE
Model
SINGLE_GROUP

Eligibility

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

Timeline & Regulatory

Start
2007-10-31
Primary Completion
2010-02-28
Completion
2010-03-31

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

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 NCT01459172 on ClinicalTrials.gov