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ACTIVE NOT RECRUITING
NCT06611553
NA

Self-collection for HPV Testing to Improve Cervical Cancer Prevention (SHIP) Trial (LMI-001-A-S02)

Sponsor: National Cancer Institute (NCI)

View on ClinicalTrials.gov

Summary

This clinical trial evaluates the use of self-collected vaginal samples for human papillomavirus (HPV) testing in patients referred for a colposcopy and/or cervical excisional procedures to improve cervical cancer prevention. HPV is a common virus which usually causes infections that last only a few months, but sometimes can last longer. It is known to cause a variety of cancers including cancer of the cervix. Even though there are ways to detect cervical cancer early, many individuals do not undergo screening that involves pelvic exams. Over half of all new cervical cancer cases are among those who have either never been screened or who are not screened enough. Without appropriate screening and care, preventable pre-cancers may turn into cancer. A new way to detect cervical cancer is to have individuals collect their own vaginal sample for HPV testing to know their risk for cervical cancer. This may give individuals more flexibility and comfort having the ability to collect samples themselves, compared to a doctor performing a speculum examination and collecting the samples in a clinic. This study compares clinical accuracy of HPV testing on self-collected vaginal samples versus cervical samples collected by clinician. The Self-collection for HPV Testing to Improve Cervical Cancer Prevention (SHIP) Trial is part of the National Cancer Institute (NCI)'s Cervical Cancer 'Last Mile' Initiative, a public private partnership that seeks to increase access to cervical cancer screening. The SHIP Trial focuses on developing clinical evidence to inform the US Food and Drug Administration (FDA)'s regulatory reviews of self-collection approaches as alternative sample collection approaches for cervical cancer screening. Several industry partner-specific self-collection device and assay combinations will be non-competitively and independently evaluated with a similar study design framework to inform pre-approval and/or post-approval regulatory requirements.

Official title: NCI Cervical Cancer 'Last Mile' Initiative 'Self-Collection for HPV Testing to Improve Cervical Cancer Prevention' (SHIP) Trial LMI-001-A-S02

Key Details

Gender

FEMALE

Age Range

25 Years - Any

Study Type

INTERVENTIONAL

Enrollment

500

Start Date

2024-09-13

Completion Date

2026-12-31

Last Updated

2025-12-15

Healthy Volunteers

No

Interventions

PROCEDURE

Biospecimen Collection

Undergo collection of cervical sample by clinician

PROCEDURE

Cervical Biopsy

Undergo cervical biopsy conducted by clinician

PROCEDURE

Colposcopy

Undergo colposcopy conducted by clinician

OTHER

Electronic Health Record Review

Ancillary studies

PROCEDURE

Endocervical Curettage

Undergo endocervical curettage conducted by clinician

PROCEDURE

Excision

Undergo cervical excisional procedure conducted by clinician

PROCEDURE

HPV Self-Collection

Undertake self-collection of vaginal sample

PROCEDURE

Human Papillomavirus Test

Undergo HPV testing of self-collected vaginal sample and cervical sample

OTHER

Questionnaire Administration

Ancillary studies

OTHER

Survey Administration

Ancillary studies

Locations (14)

University of Alabama at Birmingham Cancer Center

Birmingham, Alabama, United States

Yale University

New Haven, Connecticut, United States

University of Miami Miller School of Medicine-Sylvester Cancer Center

Miami, Florida, United States

Louisiana State University Health Science Center

New Orleans, Louisiana, United States

Johns Hopkins University/Sidney Kimmel Cancer Center

Baltimore, Maryland, United States

University of Mississippi Medical Center

Jackson, Mississippi, United States

NYP/Weill Cornell Medical Center

New York, New York, United States

UNC Lineberger Comprehensive Cancer Center

Chapel Hill, North Carolina, United States

Cleveland Clinic Foundation

Cleveland, Ohio, United States

University of Oklahoma Health Sciences Center

Oklahoma City, Oklahoma, United States

University of Pennsylvania/Abramson Cancer Center

Philadelphia, Pennsylvania, United States

UPMC-Magee Womens Hospital

Pittsburgh, Pennsylvania, United States

VCU Massey Comprehensive Cancer Center

Richmond, Virginia, United States

University of Puerto Rico

San Juan, Puerto Rico