Deep Neural Network Stratification for Use Detecting Endometriosis in Women Affected by Chronic Pelvic Pain (EndoCheck)
Launched by ASPIRA WOMEN'S HEALTH · Feb 8, 2022
Trial Information
Current as of June 27, 2025
Recruiting
Keywords
ClinConnect Summary
The EndoCheck clinical trial is studying a new way to help diagnose endometriosis, a condition that can cause chronic pelvic pain in women. Researchers are testing a special computer program, called a deep neural network, which looks for specific proteins in the body to see if they can help identify endometriosis more accurately. This study aims to show if this method can be a useful tool for doctors when diagnosing this condition.
To participate in this trial, women between the ages of 14 and 50 who are scheduled for surgery to investigate pelvic pain may be eligible. Participants will need to provide written consent and cannot be pregnant or have certain health issues, like active infections or cancers. If you join the study, you can expect to undergo tests related to your surgery, and your information will help researchers understand how well this new diagnostic tool works. This trial is currently recruiting participants and could help improve the way endometriosis is diagnosed in the future.
Gender
FEMALE
Eligibility criteria
- Inclusion Criteria:
- • 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
- Exclusion Criteria:
- • Participant is a female in a pre-menarchal state.
- • Participant is pregnant.
- • 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 participated (±3 months of study enrollment) in a clinical trial where an investigational drug/ device/ procedure was or is planned to be administered.
- • Participant has any general health or behavioral condition that, in the opinion of the investigator, should exclude the participant from participation.
- • Participant is under 14 years old or over 50 years old
About Aspira Women's Health
Aspira Women's Health is a pioneering clinical trial sponsor dedicated to advancing women's health through innovative diagnostic solutions. Focused on improving the early detection and management of gynecological conditions, Aspira leverages cutting-edge technology and robust research methodologies to develop non-invasive tests that empower women and healthcare providers. With a commitment to scientific rigor and patient-centered care, Aspira aims to enhance clinical outcomes and drive meaningful advancements in women's health across diverse populations.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Baltimore, Maryland, United States
Newark, Delaware, United States
Chandler, Arizona, United States
Greenwood, Indiana, United States
Lancaster, Pennsylvania, United States
Lynchburg, Virginia, United States
Newark, Delaware, United States
Greenwood, Indiana, United States
Moorestown, New Jersey, United States
Cincinnati, Ohio, United States
Mesa, Arizona, United States
Columbus, Georgia, United States
Greenwood, Indiana, United States
Valley Stream, New York, United States
Burbank, California, United States
Stockbridge, Georgia, United States
Newburg, Indiana, United States
Newburgh, Indiana, United States
Cincinnati, Ohio, United States
Patients applied
Trial Officials
Todd Pappas, PhD
Principal Investigator
Aspira Women's Health
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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