Dry Run of the ScreenUrSelf Trial
NCT05996796 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 38
Last updated 2023-08-18
Summary
The proposed study is the Dry Run preceding the ScreenUrSelf trial.
Conditions
- Cervical Cancer
- Cervical Intraepithelial Neoplasia
- Human Papilloma Virus
- HPV-Related Cervical Carcinoma
Interventions
- DEVICE
-
Colli-Pee Small Volumes
Women will self-collect a first-void urine sample at home upon receipt of the study package using the Colli-Pee Small Volumes (10 mL) device (Novosanis, Belgium). The collector tube is prefilled with a preservative (UCM, Novosanis, Belgium). Women will send the collector vial containing first-void urine along with the informed consent form to the laboratory at University of Antwerp using the prestamped envelope.
- DEVICE
-
Evalyn Brush
Women will self-collect a vaginal sample at home upon receipt of the study package using the Evalyn Brush device (Rovers Medical Devices, The Netherlands). Women will send the used brush along with the informed consent form to the laboratory at University of Antwerp using the prestamped envelope.
Sponsors & Collaborators
-
Antwerp University Hospital (UZA)
collaborator UNKNOWN -
Centre for Cancer Detection (CvKO)
collaborator UNKNOWN -
Sciensano
collaborator OTHER_GOV -
Universiteit Antwerpen
lead OTHER
Principal Investigators
-
Pierre Van Damme, MD, PhD · Universiteit Antwerpen
Study Design
- Allocation
- RANDOMIZED
- Purpose
- DIAGNOSTIC
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 30 Years
- Max Age
- 64 Years
- Sex
- FEMALE
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2023-04-10
- Primary Completion
- 2023-06-12
- Completion
- 2023-06-15
Countries
- Belgium
Study Locations
More Related Trials
-
Randomized Comparison of Vaginal Self Sampling for Human Papillomavirus (HPV) Testing by Standard Versus Dry Vaginal Swabs
NCT01316120 ·Status: UNKNOWN ·Phase: NA
-
Randomized Controlled Trial of Human Papillomavirus Testing in Primary Cervical Cancer Screening
NCT00479375 ·Status: COMPLETED ·Phase: NA
-
HPV Self-sampling to Improve Access to Cervical Cancer Screening for Persons With HIV and/or Underserved Individuals
NCT05528237 ·Status: ENROLLING_BY_INVITATION ·Phase: NA
-
Randomized Trial of Vaginal Self Sampling for Human Papillomavirus (HPV)
NCT01095198 ·Status: UNKNOWN ·Phase: PHASE2/PHASE3
-
Female Urine, Vaginal & Endocervical Swab & Cervical Specimen Collections for APTIMA Trichomonas Vaginalis Assay Testing
NCT01427023 ·Status: COMPLETED
-
Evaluation of the Use of the Colli-Pee Device to Collect First-void Urine for Molecular Detection of STIs
NCT02552914 ·Status: COMPLETED
-
Self-Collected Swabs for Primary Human Papilloma Virus (HPV) Screening
NCT05989464 ·Status: UNKNOWN
-
Human Papilloma Virus DNA Self-Test
NCT00266266 ·Status: COMPLETED
-
Evaluation of Dried Blood Spot for HCV RNA Testing
NCT03896087 ·Status: COMPLETED ·Phase: NA
-
The Self-Collection Study: a Study of Self-collected HPV Testing and Results Counseling
NCT01843478 ·Status: COMPLETED ·Phase: NA
-
Comparison of Self-collection Using Dry Compared to Wet Swabs for HPV Detection
NCT06213051 ·Status: NOT_YET_RECRUITING
-
Pap Smear Research Study
NCT00743626 ·Status: COMPLETED ·Phase: NA
-
Clinical Performance of Urine HPV Testing in Males
NCT06671210 ·Status: RECRUITING
-
Epidemiology of High-risk HPV Infection in Women Participating in a Pilot Screening Program for Cervical Cancer
NCT02809352 ·Status: COMPLETED
-
Point of Care Rapid STI Test Optimization and Validation Extension
NCT06566677 ·Status: COMPLETED
-
Comparing Specimen Collection Techniques to Screen for Sexually Transmitted Infections in Pregnant Women: A Pilot Study
NCT03877263 ·Status: TERMINATED ·Phase: NA
-
Clinical Study of a Single-Use, Point-of-Care Molecular Diagnostic Device for the Detection of Neisseria Gonorrhoeae (NG), Trichomonas Vaginalis (TV), and Chlamydia Trachomatis (CT) Utilizing Vaginal Swabs
NCT03596151 ·Status: TERMINATED ·Phase: NA
-
Pilots of Self-Collection for HPV DNA Detection
NCT00342511 ·Status: COMPLETED
-
Prospective Collection of Female and Male Specimens for PANTHER® System Testing
NCT01638637 ·Status: COMPLETED
-
Point-of-care Tests for Vaginal Discharge in Nepal
NCT05977491 ·Status: ACTIVE_NOT_RECRUITING ·Phase: NA
-
Prospective Evaluation of Self-Testing to Increase Screening
NCT03898167 ·Status: COMPLETED ·Phase: NA
-
HPV Typing Between Self- and Physician-sampled
NCT04472377 ·Status: COMPLETED ·Phase: NA
-
Prospective Collection of Female Specimens for Testing With Gen-Probe APTIMA (Registered Trademark) Assays
NCT01728103 ·Status: TERMINATED
-
Evaluation of the Cobas® 4800 HPV Test for the Detection of High-grade Cervical Disease
NCT00709891 ·Status: COMPLETED ·Phase: NA
-
Microscopic Images for the Development of a Rapid Vaginitis Diagnostic Device
NCT03585049 ·Status: COMPLETED