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Clinical Trial Summary

The purpose of the study is to find out if a self-administered (by the patient) Papanicolaou (Pap) smear is as accurate as a traditional Pap smear administered by a healthcare provider.


Clinical Trial Description

Papanicolaou (Pap) smears will be both self-obtained by the patient and obtained by a licensed physician, nurse practitioner, or physician assistant. Specimens will then be collected by the nurse or medical assistant who will label each specimen separately. Specimens will be blinded so that the pathologist will not know which specimen was self-collected and which provider-collected. Specimens will then be sent to our clinical laboratory provider (LabCorp) for analysis. Once results from the Pap smears are received, participants will be notified in the usual manner in our clinical practice. Finally, analysis will be conducted to ascertain whether or not a self-administered (by the patient) Pap smear is as accurate as a traditional Pap smear administered by a healthcare provider. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04093388
Study type Interventional
Source University of Alabama at Birmingham
Contact John B Waits, MD
Phone 2052772379
Email john.waits@cahabamedicalcare.com
Status Recruiting
Phase N/A
Start date April 26, 2021
Completion date August 30, 2025

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