Clinical Trials Directory

Trials / Withdrawn

WithdrawnNCT07211204

Comparison Of Cytology And Molecular Screening For Detecting Cervical Reactive Cellular Changes In General Population

Study To Compare The Efficacy Of Cervical Cytology With Molecular Screening In The Detection Of Reactive Cellular Changes In The Cervix In An Open Population

Status
Withdrawn
Phase
N/A
Study type
Interventional
Enrollment
0 (actual)
Sponsor
Timser SAPI de CV · Industry
Sex
Female
Age
18 Years – 85 Years
Healthy volunteers
Accepted

Summary

This study compares the efficacy of cytology (Pap smear) with the molecular screening in their ability to detect reactive cellular changes in the cervix among an open population

Detailed description

The primary goal of this study is to compare the efficacy of the cytology (Pap smear) with the molecular screening -of three human biomarkers- in their ability to detect reactive cellular changes in the cervix among an open population. Participants will be asked to attend two study visits. All the clinical procedures will be done on the first visit: 1. Explanation of the study and its procedures. Only participants that give their written Informed Consent will be enrolled in the study. 2. Interview and physical examination to obtain a medical record. The interview will collect information related to known risks factors for cervical lesions. 3. Venipuncture to obtain a blood sample. 4. Colposcopy to obtain a cervical smear and a colposcopic diagnosis. The cervical smear will be used to perform liquid-based cytology and HPV detection. 5. Biopsy, only if the gynecologist detects a cervical lesion or another abnormality during colposcopy. The gynecologist will make preliminary recommendations based on the colposcopic findings. During the second visit the study's gynecologist will explain the tests' results and provide clinical recommendations to each participant. The sensitivity, specificity, and predictive values of cytology, HPV detection, and molecular screening will be calculated using colposcopy (for all participants) and histopathology (for those biopsied). These results will be compared using a DeLong test. Correlation tests will be performed using risk factors data and test results.

Conditions

Interventions

TypeNameDescription
PROCEDUREPhysical examinationPhysical examination and interview for obtaining a medical record
OTHERLiquid-based cytologyScreening test for cervical precursor lesions and/or cancer. LBC is a procedure in which a cervical smear is examined under the microscope.
OTHERMolecular screeningThe molecular screening detects three human biomarkers associated with cervical precursor lesions and/or cervical cancer. Biomarker detection is done by Western blot and ELISA in human sera.
OTHERHPV DNA testHPV DNA detection is performed using a cervical swab.
DIAGNOSTIC_TESTColposcopyA diagnostic procedure to visually examine the cervix, vagina, and vulva with a colposcope.
DIAGNOSTIC_TESTHistopathologyIs the definitive diagnosis of cervical precursor lesions and cervical cancer. It is the microscopic study of diseased cells and tissues stained with hematoxylin and eosin.

Timeline

Start date
2026-02-27
Primary completion
2026-02-27
Completion
2026-02-27
First posted
2025-10-07
Last updated
2026-03-03

Locations

1 site across 1 country: Mexico

Source: ClinicalTrials.gov record NCT07211204. Inclusion in this directory is not an endorsement.