Actively Recruiting
Comparison Between Liquid-Based Cytology And Molecular Screening For Detecting Precursor Lesions and Cervical Cancer
Led by Timser SAPI de CV · Updated on 2026-03-18
558
Participants Needed
1
Research Sites
16 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This study compares how effective is the molecular screening (a blood test) using Pap smear as reference, that is, a comparison of these tests abilities to detect precursor lesions and cervical cancer among women of an open population
CONDITIONS
Official Title
Comparison Between Liquid-Based Cytology And Molecular Screening For Detecting Precursor Lesions and Cervical Cancer
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Be in good general health
- Aged between 18 and 85 years
- Fast for at least 6 hours and no more than 12 hours before the study
- Avoid sexual intercourse for 24 hours before the study
- Provide written informed consent
You will not qualify if you...
- Have had subtotal, total, or radical hysterectomy
- Are pregnant or suspect pregnancy
- Currently undergoing oncological treatment such as chemotherapy, radiotherapy, or brachytherapy
- Are menstruating during the study
- Have a confirmed diagnosis of HIV or hepatitis infection
- Have taken antiplatelet medications, like acetylsalicylic acid, within 24 hours before the study
AI-Screening
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Trial Site Locations
Total: 1 location
1
Consultorio Médico TIMSER
Mexico City, Mexico City, Mexico, 14210
Actively Recruiting
Research Team
M
Mercedes Gutiérrez-Smith, Bachelor of Arts in History
CONTACT
F
Fátima R Ruiz-Rosales, Bachelor of Medicine
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
TRIPLE
Allocation
NON_RANDOMIZED
Model
PARALLEL
Primary Purpose
SCREENING
Number of Arms
2
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