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OpenTrials
Active, Not Recruiting

NCT Number: NCT02811224

Ovarian Cancer Hemoscope Trial

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.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

Key information

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

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

Exclusion criteria

  • Previous cancer diagnosis (all)
  • 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

Treatment and study plan

Primary outcomes

  1. Sensitivity of an assay that detects circulating tumor DNA

    Time frame: 3 years

Sponsors and collaborators

Lead sponsor

Scripps Translational Science Institute

Other

Registry information

Important dates

Study start
2016
Primary completion
2025
Study completion
2030
First posted
Jun 23, 2016
Registry last updated
Jan 16, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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