Endometrial Cancer Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- People who are willing and able to give documented informed consent to participate
- People who are 25 years of age or older
- People who have a cervix that has not been removed or surgically altered
- People who have been referred for a colposcopy procedure because recent cervical cancer screening (within the past 12 months) showed a positive HPV test, an unclear cell result (ASC-US), or abnormal cell results — or who have been referred for a cervical excisional procedure
- People who are willing and able to undergo a colposcopy, and if the treating doctor determines it is medically necessary, also a biopsy, endocervical curettage (sampling of the cervical canal), and/or a cervical excisional procedure
Who may not be able to join:
- People who are currently pregnant or who gave birth within the past 3 months
- People who have had a treatment to the cervix in the past 12 months — such as a LEEP procedure, cone biopsy, laser surgery, cryotherapy, or thermal ablation
- People who have had a full or partial hysterectomy, including any surgery that removed the cervix, either by self-report or confirmed through medical records
- People with known medical conditions that the trial investigator determines would prevent safe participation (confirm with trial site)
- People who have previously taken part in the SHIP Trial or another cervical cancer screening study within the past 12 months, where participation included completing a self-collection
- People who are currently experiencing unusual bleeding or pelvic pain
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Clinical sensitivity for self-collected (SC) samples; Clinical sensitivity for clinician-collected (CC) samples; Clinical specificity for SC samples; Clinical specificity for CC samples; False positive rate (FPR) for SC samples; FPR for CC samples; False negative rate (FNR) for SC samples; FNR for CC samples; Sensitivity ratio for SC versus CC samples; Specificity ratio for SC versus CC samples; False positive (FP) ratio for SC versus CC samples; False negative (FN) ratio for SC versus CC samples; Positive percent agreement; Negative percent agreement
Can't join this trial?
Data last synced from ClinicalTrials.gov: 21 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.