Collection of Outcomes Data for Pregnant Patients With Cancer
| Status: | Recruiting |
|---|---|
| Conditions: | Cancer, Women's Studies |
| Therapuetic Areas: | Oncology, Reproductive |
| Healthy: | No |
| Age Range: | Any |
| Updated: | 9/16/2018 |
| Start Date: | December 2005 |
| End Date: | December 2020 |
| Contact: | Sue Rimes, RN |
| Phone: | 713-563-4546 |
You are being asked to take part in this study because you are pregnant or have been pregnant
while diagnosed with cancer.
The goal of this research study is to collect information on patients who are or were
pregnant while diagnosed with cancer and to store this information in a research database.
This is an investigational study. About 500 patients will take part in this study. All will
be enrolled at MD Anderson.
while diagnosed with cancer.
The goal of this research study is to collect information on patients who are or were
pregnant while diagnosed with cancer and to store this information in a research database.
This is an investigational study. About 500 patients will take part in this study. All will
be enrolled at MD Anderson.
If you agree to take part in this study, information about the type of cancer, the type of
treatment you have had or are having, and details about your pregnancy will be collected for
the database. Data will be collected from patients seen at MD Anderson since September 2003
until data has been collected for 500 cases. This information will serve as a basis for
future studies about pregnant women with cancer. You will receive no special tests or
treatment at MD Anderson as a result of this study.
Progress notes and ultrasound reports about your pregnancy will be requested from Maternal
Fetal Medicine and/or from your personal obstetrician. This information will be entered into
the database and also included in your medical record. If the information is not consistent
in the record, we may contact you to clarify the information. You will remain on study until
your pregnancy and/or any treatment you are receiving are completed.
Periodically the database will be updated to include information about patient survival. This
information is usually found in the medical record however it may be necessary to contact you
directly.
treatment you have had or are having, and details about your pregnancy will be collected for
the database. Data will be collected from patients seen at MD Anderson since September 2003
until data has been collected for 500 cases. This information will serve as a basis for
future studies about pregnant women with cancer. You will receive no special tests or
treatment at MD Anderson as a result of this study.
Progress notes and ultrasound reports about your pregnancy will be requested from Maternal
Fetal Medicine and/or from your personal obstetrician. This information will be entered into
the database and also included in your medical record. If the information is not consistent
in the record, we may contact you to clarify the information. You will remain on study until
your pregnancy and/or any treatment you are receiving are completed.
Periodically the database will be updated to include information about patient survival. This
information is usually found in the medical record however it may be necessary to contact you
directly.
Inclusion Criteria:
1. All pregnant patients with cancer and patients known to have been pregnant with a
diagnosis of cancer are eligible, regardless of their diagnosis or treatment plan.
2. Patients may receive prenatal care from any obstetrician, but a consult with Maternal
Fetal Medicine is encouraged.
Exclusion Criteria:
We found this trial at
1
site
1515 Holcombe Blvd
Houston, Texas 77030
Houston, Texas 77030
713-792-2121
Principal Investigator: Andrea Milbourne, MD
University of Texas M.D. Anderson Cancer Center The mission of The University of Texas MD...
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