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TERMINATEDNANCT01716052

Women's Mammography Study To Improve Comfort During Mammography

The purpose of this study is to determine in a randomized trial whether it is possible to decrease the discomfort of mammography by using the analgesic ibuprofen, or by using a scripted, supportive te...

Lead sponsor: Kenneth A. Kist,•1 U.S. locations•View source on ClinicalTrials.gov

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Sponsors

Lead Sponsor

Kenneth A. Kist,

This study is designed to evaluate two methods of reducing pain and discomfort caused by mammography, one of the barriers to the procedure.

Age

18 - 100 years

Sex

FEMALE

Healthy Volunteers

Yes

Inclusion Criteria

•Must have signed the informed consent.
•Must either be getting her first mammogram or based on prior experience be expecting level 4 or 5 pain

Exclusion Criteria

•May not have taken ibuprofen or other pain medication within the last 12 hours.
•Must not have a contraindication for taking ibuprofen e.g:
•No history of allergic reactions to ibuprofen or aspirin
•No recent history with the last year of bleeding from GI tract
•Not pregnant or suspected of being pregnant

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Data from ClinicalTrials.govLast updated on ClinicalTrials.gov: December 30, 2015Terms

Trial snapshot

StatusTERMINATED

PhaseNA

Enrollment2

Start dateJul 2012

Last updatedDec 30, 2015

Condition

Locations shown

Cancer Therapy and Research Center at UTHSCSA

San Antonio, Texas

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Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: December 30, 2015Data synced to Clareo: May 10, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

View ClinicalTrials.gov Terms and Conditions