Use of the CA 125 Algorithm for the Early Detection of Ovarian Cancer in Low Risk Women
-
- STATUS
- Recruiting
-
- End date
- Jul 31, 2023
-
- participants needed
- 8000
-
- sponsor
- M.D. Anderson Cancer Center
Summary
The goal of this clinical research study is to evaluate a method involving a blood test, called CA-125, that may be helpful in the early detection of ovarian cancer in women who are at low risk.
Description
Currently, there is no effective screening to detect ovarian cancer at its earliest stage in low risk women. CA-125 is an FDA approved blood test that may show the presence of ovarian cancer.
If you are eligible to take part in this research study:
- You will have blood (about 2-3 tablespoons) drawn for CA-125 testing and other tumor markers. Tumor markers may be related to the presence of certain cancers.
- You will be asked to complete a questionnaire about your medical and family history. It should take about 20-30 minutes to complete.
- You will be asked to complete a questionnaire about your symptoms. It should take about 10-15 minutes to complete.
Depending on your CA-125 level:
- You will have blood (about 2-3 tablespoons) drawn for CA-125 testing and other tumor markers in 1 year.
- You will have blood (about 2-3 tablespoons) drawn for CA-125 testing and other tumor markers in 3 months, OR
- You will have blood (about 2-3 tablespoons) drawn for CA-125 testing and other tumor markers, and you will have a transvaginal ultrasound (to look at your ovaries and fallopian tubes) in 6 weeks +/- 2 weeks.
An ultrasound test uses sound waves to check the position, size, and shape of the ovaries. During a transvaginal ultrasound, a small probe will be placed in your vagina and used to create and measure sound waves.
Based on the results of the transvaginal ultrasound (if you receive one):
- You and the study doctor will discuss options for further treatment or standard cancer management, OR
- You will have blood (about 2-3 tablespoons) drawn for CA-125 testing and other tumor markers in 3 months.
When you return for your next visit (at 1 year, 3 months, or 6 weeks +/- 2 weeks), and each visit after that:
- You will have blood (about 2-3 tablespoons) drawn for CA-125 testing and other tumor markers.
- You will be asked to complete the questionnaire about your symptoms.
- You will be asked to complete a follow-up visit survey so that any updates to your personal and family medical history can be recorded. It should take about 10 minutes to complete.
Your CA-125 blood draw results will be sent to you by letter or e-mail so that you will know when to return for a visit.
If you miss a visit, the study staff may try to contact you by telephone, e-mail, or letter. Visit reminders may also be sent to you by letter or e-mail.
Length of Study:
You will continue to return for visits depending on the CA-125 level from your last visit. If you are unable to return for visits after 3 years, you will be taken off study. You may continue to take part in this study unless you no longer qualify for the study or you no longer would like to take part in this study.
This is an investigational study. Transvaginal ultrasound scans on this study are performed using FDA-approved and commercially available methods.
Up to 8,000 women will take part in this multicenter study. Up to 2,000 will be enrolled at MD Anderson.
Details
| Condition | Ovarian Cancer |
|---|---|
| Treatment | Questionnaire, transvaginal ultrasound, CA 125 Analysis |
| Clinical Study Identifier | NCT00539162 |
| Sponsor | M.D. Anderson Cancer Center |
| Last Modified on | 16 October 2022 |
How to participate?
,
You have contacted , on
Your message has been sent to the study team at ,
What happens next?
- You can expect the study team to contact you via email or phone in the next few days.
- Sign up as volunteer to help accelerate the development of new treatments and to get notified about similar trials.
You are contacting
Primary Contact
Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.
Learn moreIf you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.
Learn moreComplete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.
Learn moreSimilar trials to consider
Browse trials for
Not finding what you're looking for?
Sign up as a volunteer to stay informed
Every year hundreds of thousands of volunteers step forward to participate in research. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.
Sign up as volunteer