Actively Recruiting
Rice Technologies for Cervical Cancer Screening and Diagnosis
Led by M.D. Anderson Cancer Center · Updated on 2026-02-13
678
Participants Needed
4
Research Sites
366 weeks
Total Duration
On this page
Sponsors
M
M.D. Anderson Cancer Center
Lead Sponsor
E
Eduardo Mondlane University
Collaborating Sponsor
AI-Summary
What this Trial Is About
The study aims to compare the accuracy of the lateral flow test to detect HPV at the POC with commercially available HPV test and to determine the diagnostic accuracy and reliability of a multimodal optical imaging system to detect cervical dysplasia, with the gold reference standard of histopathology.
CONDITIONS
Official Title
Rice Technologies for Cervical Cancer Screening and Diagnosis
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Women aged 25 to 49 years
- Women with a positive cervical cancer screening test (abnormal cytology, positive VIA, or positive HPV test)
- Women with an intact cervix
- Women who are not pregnant and have a negative pregnancy test within 14 days of enrollment and are not currently breastfeeding
- Women willing and able to provide informed consent
You will not qualify if you...
- Women under 25 or over 49 years old
- Women who have had a total hysterectomy including removal of the cervix
- Women who are pregnant or breastfeeding
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 4 locations
1
M D Anderson Cancer Center
Houston, Texas, United States, 77030
Actively Recruiting
2
José Macamo General Hospital and Health Center
Maputo, Mozambique, 1106
Actively Recruiting
3
Maputo Central Hospital
Maputo, Mozambique, 1106
Actively Recruiting
4
Mavalane Hospital and Health Center
Maputo, Mozambique, 1108
Actively Recruiting
Research Team
M
Mila Salcedo, MD, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
SCREENING
Number of Arms
1
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