Vaginal Fluid Collection Study for Endometrial Cancer Test Research and Development

Status: Recruiting
Location: See location...
Intervention Type: Diagnostic test
Study Type: Observational
SUMMARY

The primary objective of this study is to obtain de-identified vaginal fluid specimens from participants with an endometrial tissue biopsy-based histopathological diagnosis of endometrial cancer (EC), endometrial hyperplasia (AEH) with atypia or endometrial intraepithelial neoplasia (EIN). The samples will be used for the purpose of research and development of a new molecular diagnostic test for the detection of EC, AEH and EIN.

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 18
Healthy Volunteers: f
View:

• Women ≥18 years of age.

• Women with endometrial tissue biopsy-based histopathological diagnosis of EC (any histology, including uterine carcinosarcoma), AEH or EIN.

• Women whose planned surgical intervention (if any) includes hysterectomy, D\&C, or hysteroscopic resection.

• Participant understands the study procedures and can provide informed consent to participate in the study and authorization for release of relevant protected health information to the study Investigator.

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Locations
United States
Louisiana
Trials365
RECRUITING
Shreveport
Contact Information
Primary
Wallis Blumm
wblumm@innovis.net
9172082989
Backup
Gregg S Britt
gbritt@innovis.net
3103863000
Time Frame
Start Date: 2024-02-19
Estimated Completion Date: 2024-06-01
Participants
Target number of participants: 40
Related Therapeutic Areas
Sponsors
Leads: Innovis LLC

This content was sourced from clinicaltrials.gov