NCT05245695Recruiting
Deep Neural Network Stratification for Use Detecting Endometriosis in Women Affected by Chronic Pelvic Pain (EndoCheck)
Deep Neural Network Stratification for the Use in Detecting Endometriosis in Women Affected by Chronic Pelvic Pain (EndoCheck)
Source: ClinicalTrials.gov · Last updated 28 Oct 2026
Brief summary (registry, in English)
The goal of this observational study is to determine the clinical validity of a deep neural network algorithm that utilizes protein biomarker detection of Endometriosis - "EndoCheck" - as an "aid in diagnosis" for endometriosis and to show validity as a diagnostic test
- Status (registry)
- Recruiting
- Study type
- Observational
- Enrollment
- 1200 (estimated)
- First submitted
- 1 Feb 2022
- Start date
- 12 Jul 2022
- Primary completion date
- 30 Nov 2026
- Lead sponsor
- Aspira Women's Health
- Diseases
- Endometriosis
- NCT number
- NCT05245695
What you commit to
- Study type: Observational
- Planned participants: 1200
- From 12 Jul 2022 to the primary completion date, 30 Nov 2026
- 10 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Participant has participated (±3 months of study enrollment) in a clinical trial where an investigational drug/ device/ procedure was or is planned to be administered.
Other illness
- Participant has an active malignancy.
- Participant is known to have tested positive for human immunodeficiency virus or hepatitis A, B, or C.
- Participant has an active pelvic infection or other infections contraindicated for surgery.
- Participant has any general health or behavioral condition that, in the opinion of the investigator, should exclude the participant from participation.
Age
- Participant is under 14 years old or over 50 years old
Other
- Participant is a female in a pre-menarchal state.
- Participant is pregnant.
Who the study is looking for
- Participant is willing and able to provide written informed consent.
- Participant is a female aged 14 to 50 years old at time of consent.
- Participant is scheduled to undergo laparotomy or laparoscopy for symptomology consistent with possible endometriosis
Age in the registry: 14 years to 50 years · Sex: Female · Does not accept healthy volunteers
Sites (10)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Johns Hopkins School of Medicine Coordinator of this site? Confirm its status | Baltimore | United States | Recruiting |
| Velvet Clinical Research Coordinator of this site? Confirm its status | Burbank | United States | Recruiting |
| New Horizons Clinical Trials Coordinator of this site? Confirm its status | Chandler | United States | Recruiting |
| Seven Hills Clinical Research Coordinator of this site? Confirm its status | Cincinnati | United States | Recruiting |
| Midtown OBGYN North Coordinator of this site? Confirm its status | Columbus | United States | Recruiting |
| Cindy Basinski, MD Coordinator of this site? Confirm its status | Forest Hill | United States | Recruiting |
| Womens Health Services of Central Virginia Coordinator of this site? Confirm its status | Lynchburg | United States | Recruiting |
| Reproductive Associates of Delaware (RAD) Coordinator of this site? Confirm its status | Newark | United States | Recruiting |
| Advanced Women's Care Center Coordinator of this site? Confirm its status | Stockbridge | United States | Recruiting |
| Nezhat Surgery for Gynecology/Oncology Coordinator of this site? Confirm its status | Valley Stream | United States | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.