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Data Collection for Patients With Low Grade Ovarian or Peritoneal Tumors

Data Collection for Patients With Low Grade Ovarian Carcinoma

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00488878
Enrollment
2000
Registered
2007-06-20
Start date
2006-05-19
Completion date
2035-05-01
Last updated
2026-08-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Low Grade Ovarian Serous Adenocarcinoma, Malignant Ovarian Neoplasm, Ovarian Carcinoma, Primary Peritoneal Carcinoma, Primary Peritoneal Low Grade Serous Adenocarcinoma, Psammocarcinoma

Brief summary

This study collects information to maintain a database on patients with low-grade ovarian or peritoneal tumors. Collecting information about the type of cancer and treatment, as well as details about follow-up care, may help researchers learn and better understand these tumor types and help develop better treatments for them.

Detailed description

PRIMARY OBJECTIVES: I. To collect, both prospectively and retrospectively, data on disease characterization, treatment, and outcomes for approximately 1600 female patients with low-grade ovarian and peritoneal tumors. II. To organize clinical information in order to support multifaceted queries of patient characteristics, treatment, and disease 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. SECONDARY OBJECTIVE: I. To obtain and store human tumor samples in the form of blocks or slides for the purpose of establishing a tumor bank. OUTLINE: Patients' medical records are reviewed for retrospective and prospective data collection. Patients may also have residual tissue samples collected and stored.

Interventions

PROCEDUREBiospecimen Collection

Patients' residual tissue samples are collected

OTHERElectronic Health Record Review

Medical records are reviewed

Sponsors

M.D. Anderson Cancer Center
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
OTHER

Eligibility

Sex/Gender
FEMALE
Healthy volunteers
No

Inclusion criteria

* Patients whose disease progressed to a higher-grade carcinoma since the time of original diagnosis: * Ovarian tumor of low malignant potential * Low-grade serous carcinoma of the ovary * Primary peritoneal tumor of low malignant potential * Low-grade serous carcinoma of the peritoneum * Psammocarcinoma

Design outcomes

Primary

MeasureTime frameDescription
Prospective and retrospective data collection on disease characterization, treatment, and outcomesUp to 28 years
Organization of clinical informationUp to 28 yearsWill be done in order to support multifaceted queries of patient characteristics, treatment, and disease outcome data and to facilitate correlation of these characteristics with patient outcome.
Creation of a single data repository to integrate clinical information and research findingsUp to 28 years

Secondary

MeasureTime frame
Collection and storage of human tumor samples for the establishment of a tumor bankUp to 28 years

Countries

United States

Contacts

CONTACTLisa Nathan
lcnathan@mdanderson.org713-745-3837
PRINCIPAL_INVESTIGATORDavid M Gershenson

M.D. Anderson Cancer Center

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 11, 2026