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DOvEE - Diagnosing Ovarian & Endometrial Cancer Early

Ovarian Neoplasms

This study hopes to improve early detection of ovarian and endometrial cancers. It will determine if women with bloating, abdominal distension, abdominal/pelvic pain, increased urinary frequency and/or early satiety, benefit from earlier surgery after screening by CA-125 ovarian cancer biomarker and transvaginal ultrasound.

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Participation Requirements

  • Sex:

    FEMALE
  • Eligible Ages:

    45 and up

Participation Criteria

Inclusion Criteria:

1. Sign an approved informed consent form (ICF).
2. Be ≥ 45 years of age.
3. Have at least one symptom outlined in below for a period of ≥2 weeks but ≤ 1 year:

* Feeling full after eating only a few bites, loss of appetite
* Diarrhea, constipation, bowel or rectum feels full, change in bowel habits, constant urge to have a bowel movement, painful or burning bowel movements, rectal pain, painful defecation
* Bloating, distension of abdomen, clothes around the waist feel too tight, feel an abdominal mass
* Weight loss not because of dieting
* Nausea, vomiting, heartburn, gas, burping, indigestion
* Increased urinary frequency, need to urinate urgently, pressure on the bladder, leaking urine, burning sensation when urinating, need to urinate but unable to do so, unable to empty bladder completely, feeling full after urinating
* Vaginal discharge, bleeding, spotting, deep pain on intercourse
* Discomfort or pain in abdomen, or pelvic region, or lower back
4. Subjects must be willing to comply with study protocol

Exclusion Criteria:

1. Previous bilateral salpingo-oophorectomy (BSO)
2. Previous diagnosis of cancer in the ovaries, fallopian tubes, or peritoneum
3. Current bleeding per rectum, not due to haemorrhoids
4. Current frank haematuria
5. Symptoms that suggest the need for urgent clinical evaluation outside of a research protocol

Study Location

West Island Cancer Wellness Centre
West Island Cancer Wellness Centre
Kirkland, Quebec
Canada

Contact Study Team

McGill University Health Centre, Royal Victoria Hospital
McGill University Health Centre, Royal Victoria Hospital
Montreal, Quebec
Canada

Contact Study Team

Primary Contact

Lucy Gilbert, MD,MSc,FRCOG

[email protected]
514-934-1934
Backup Contact

Claudia Martins, MD, PhD

[email protected]
514-934-1934
Clinique Médicale du Haut-Anjou
Clinique Médicale du Haut-Anjou
Montreal, Quebec
Canada

Contact Study Team

Clinique du Dr. L. Quintal
Clinique du Dr. L. Quintal
St Lambert, Quebec
Canada

Contact Study Team

Clinique Familiale Pas-A-Pas
Clinique Familiale Pas-A-Pas
Montreal, Quebec
Canada

Contact Study Team

Lachine Hospital
Lachine Hospital
Montreal, Quebec
Canada

Contact Study Team

Axion 50 plus
Axion 50 plus
Laval, Quebec
Canada

Contact Study Team

Queen Elizabeth Health Centre
Queen Elizabeth Health Centre
Montreal, Quebec
Canada

Contact Study Team

Backup Contact

Claudia Martins, MD, PhD

Primary Contact

Lucy Gilbert, MD MSc FRCOG

Study Sponsored By
McGill University
Participants Required
More Information
Study ID: NCT02296307