SELF-CERV Pivotal Study: SELF-Collection for CERVical Cancer Screening
Public ClinicalTrials.gov record NCT06120205. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.
Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.
Official title
SELF-CERV Pivotal Study: Method Comparison of Self-collection Using the Teal Wand Self-Collection Device and HCP (Health Care Provider) Cervical Collection for Detection of High-risk HPV (hrHPV) for Cervical Cancer Screening
Study identification
- NCT ID
- NCT06120205
- Recruitment status
- Active, not recruiting
- Study type
- Interventional
- Phase
- Not applicable
- Lead sponsor
- Teal Health, Inc.
- Industry
- Enrollment
- 870 participants
Conditions and interventions
Conditions
Interventions
- Teal Wand Self-Collection Device Group Device
Device
Eligibility (public fields only)
- Age range
- 25 Years to 65 Years
- Sex
- Female
- Healthy volunteers
- Accepts healthy volunteers
This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.
Study timeline
- Start date
- Nov 19, 2023
- Primary completion
- Apr 4, 2024
- Completion
- May 31, 2027
- Last update posted
- Jul 17, 2025
2023 – 2027
United States locations
- U.S. sites
- 15
- U.S. states
- 12
- U.S. cities
- 13
| Facility | City | State | ZIP | Site status |
|---|---|---|---|---|
| Birmingham OBGYN / Alabama Clinical Therapeutics | Birmingham | Alabama | 35235 | — |
| Planned Parenthood Northern California | San Francisco | California | 94109 | — |
| University of Colorado Anschutz Medical Campus | Aurora | Colorado | 80045 | — |
| Planned Parenthood Southern New England | New Haven | Connecticut | 06511 | — |
| Yale University | New Haven | Connecticut | 06520 | — |
| Woman's Hospital | Baton Rouge | Louisiana | 70817 | — |
| Johns Hopkins University | Baltimore | Maryland | 21287 | — |
| Planned Parenthood League of Massachusetts | Boston | Massachusetts | 02215 | — |
| Planned Parenthood St. Louis Region | St Louis | Missouri | 62208 | — |
| Washington University | St Louis | Missouri | 63110 | — |
| New York University Langone Hospital | Mineola | New York | 11501 | — |
| Unified Women's Clinical Research Raleigh | Raleigh | North Carolina | 27607 | — |
| Unified Women's Clinical Research - Lyndhurst | Winston-Salem | North Carolina | 27103 | — |
| Planned Parenthood Gulf Coast | Houston | Texas | 77023 | — |
| University of Wisconsin - Madison | Madison | Wisconsin | 53715 | — |
Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.
About this trial record page
- What this page shows
- Public field values for ClinicalTrials.gov record NCT06120205, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
- What this page does not do
- No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
- Where the data comes from
- Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
- Last refresh
- Last update posted Jul 17, 2025 · Synced Apr 29, 2026
Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.
Open the official record
The complete protocol, eligibility criteria, and contact information for NCT06120205 live on ClinicalTrials.gov.