NCT04915495

Brief Summary

This study is designed to demonstrate that a multimodal hyperspectral device (LuViva) is able to segregate women with abnormal screening tests into Low and High risk groups for the purpose of determining whether they require enhanced colposcopy and additional biopsies in order to increase detection of CIN2+ cervical disease.

Trial Health

55
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
400

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started May 2023

Typical duration for not_applicable

Geographic Reach
1 country

4 active sites

Status
enrolling by invitation

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

May 28, 2021

Completed
10 days until next milestone

First Posted

Study publicly available on registry

June 7, 2021

Completed
1.9 years until next milestone

Study Start

First participant enrolled

May 5, 2023

Completed
2.2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 31, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

July 31, 2025

Completed
Last Updated

March 21, 2025

Status Verified

March 1, 2025

Enrollment Period

2.2 years

First QC Date

May 28, 2021

Last Update Submit

March 19, 2025

Conditions

Keywords

Cervical cancer, dysplasia, detection

Outcome Measures

Primary Outcomes (1)

  • Sensitivity of Diagnostic Device

    LuViva's ability to correctly identify diseased tissue. LuViva result indicated High-risk and the pathology results indicate the presence of disease cervical tissue.

    up to 60 days after completion of enrollment

Secondary Outcomes (1)

  • Specificity of Diagnostic Device

    up to 60 days after completion of enrollment

Study Arms (1)

Singe-arm Study

EXPERIMENTAL

Experimental device being evaluated for sensitivity and specificity.

Diagnostic Test: LuViva Advanced Cervical Scan

Interventions

Multimodal hyperspectral device

Singe-arm Study

Eligibility Criteria

Age18 Years+
Sexfemale
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Able to read or understand and give informed consent
  • Referral Pap test within 120 days
  • Scheduled for colposcopy based on the 2019 ASCCP Management Guidelines that fall within the 4% to 59% Immediate CIN3+ risk with the exception of women who lack a cervix or may be pregnant and are recommended to colposcopy.\*

You may not qualify if:

  • Pregnancy
  • Menstruating on the day of colposcopy and LuViva test
  • Radiation therapy to her genitourinary system within 1 year
  • Prior hysterectomy in which cervix was removed
  • Congenital anatomical cervical variant (e.g., double cervix)
  • Friable cervix at the time of the study (i.e., a cervix that bleeds easily upon minimal contact or trauma)
  • Post-coital or other significant bleeding at the time of the exam
  • Excessive cervical mucous or discharge that cannot be removed and is significant enough, in the opinion of the Investigator, to interfere with a Pap test or colposcopy, resulting from inflammation, bacterial infection or other sources
  • History of any photosensitizing disease or other disease affected by Ultra-violet radiation, (e.g., pophyria, Lupus Erythematosus).
  • Undergoing phototherapy
  • Recent use of photosensitizing agents, such as fluoroquinolones or retinoids
  • Under-screened populations - defined as those women who have not been screened within the past 5 years who also screen positive for any HPV genotype

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (4)

University of Alabama Birmingham- Heersink School of Medicine

Birmingham, Alabama, 35233, United States

Location

Emory University- Winship Cancer Institute

Atlanta, Georgia, 30322, United States

Location

Great Lakes Bay Health Centers

Bay City, Michigan, 48706, United States

Location

Tidewater Clinical Research

Norfolk, Virginia, 23502, United States

Location

Related Publications (23)

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    PMID: 32243307BACKGROUND
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MeSH Terms

Conditions

Uterine Cervical DysplasiaUterine Cervical Neoplasms

Condition Hierarchy (Ancestors)

Precancerous ConditionsNeoplasmsUterine Cervical DiseasesUterine DiseasesGenital Diseases, FemaleFemale Urogenital DiseasesFemale Urogenital Diseases and Pregnancy ComplicationsUrogenital DiseasesGenital DiseasesUterine NeoplasmsGenital Neoplasms, FemaleUrogenital NeoplasmsNeoplasms by Site

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
DIAGNOSTIC
Intervention Model
SINGLE GROUP
Sponsor Type
INDUSTRY
Responsible Party
SPONSOR

Study Record Dates

First Submitted

May 28, 2021

First Posted

June 7, 2021

Study Start

May 5, 2023

Primary Completion

July 31, 2025

Study Completion

July 31, 2025

Last Updated

March 21, 2025

Record last verified: 2025-03

Data Sharing

IPD Sharing
Will not share

Locations