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NCT02811224Active, not recruiting

Ovarian Cancer Hemoscope Trial

Source: ClinicalTrials.gov · Last updated 16 Jan 2025

Brief summary (registry, in English)

This is a prospective, gold standard observational trial designed to enroll consecutive, consenting ovarian cancer patients for the purpose of determining sensitivity of an assay that detects circulating tumor DNA. This observational pilot trial will also be used to examine the genetic variants/mutations present in the tumor tissue DNA.

Status (registry)
Active, not recruiting
Study type
Observational
Enrollment
50 (estimated)
First submitted
21 Jun 2016
Start date
1 May 2016
Primary completion date
30 Jun 2025
Lead sponsor
Scripps Translational Science Institute
NCT number
NCT02811224

What you commit to

  • Study type: Observational
  • Planned participants: 50
  • From 1 May 2016 to the primary completion date, 30 Jun 2025
  • No sites listed in no 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

  • Radiation therapy before surgical treatment
  • Bone marrow transplant
  • Chemotherapy before surgical treatment
  • Invasive procedure resulting in damage to tissue (e.g., surgery, biopsy, thermal ablation) in the 7 days prior to baseline (pre-surgical) blood collection

Other illness

  • Previous cancer diagnosis (all)

Who the study is looking for

  • Case Group
  • Patients with ovarian cancer undergoing surgery (all stages)
  • Over 18 years old
    • Control Group
  • Patients with a benign gynecological condition undergoing surgery
  • Over 18 years old

Age in the registry: 18 years to - · Sex: Female · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

This page is information, not medical advice. Discuss any trial with your doctor.