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Clinical Trials/NCT00507572
NCT00507572
Terminated
Not Applicable

Collection of Outcomes Data for Pregnant Patients With Cancer

M.D. Anderson Cancer Center1 site in 1 country313 target enrollmentDecember 19, 2005

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Hematopoietic and Lymphoid Cell Neoplasm
Sponsor
M.D. Anderson Cancer Center
Enrollment
313
Locations
1
Primary Endpoint
Creation of data repository for patient characteristics, treatment, and pregnancy outcome data
Status
Terminated
Last Updated
8 months ago

Overview

Brief Summary

This study collects treatment and outcomes information on pregnant patients who are or were pregnant with cancer. Gathering and storing health information on pregnant patients with cancer, may provide data for future research studies and improve patient care.

Detailed Description

PRIMARY OBJECTIVES: I. To collect, both prospectively and retrospectively, data on disease characterization, treatment and outcome for pregnant patients with malignancies seen at M. D. Anderson Cancer Center. II. To organize clinical information in order to support multifaceted queries of patient characteristics, treatment, and pregnancy outcome data and to facilitate correlation of these characteristics with patient outcome. III. To have a single data repository, kept on a secure platform, that will integrate clinical information and research findings and serve as a secure archive for future research. OUTLINE: Patients' medical records are reviewed prospectively and retrospectively.

Registry
clinicaltrials.gov
Start Date
December 19, 2005
End Date
August 8, 2025
Last Updated
8 months ago
Study Type
Observational
Sex
Female

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • 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
  • Patients may receive prenatal care from any obstetrician, but a consult with Maternal Fetal Medicine is encouraged

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Creation of data repository for patient characteristics, treatment, and pregnancy outcome data

Time Frame: Up to 15 years

Study Sites (1)

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