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Recruiting

NCT Number: NCT00488878

Data Collection for Patients With Low Grade Ovarian or Peritoneal Tumors

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.

Recruiting

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Key information

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Biospecimen Collection

Procedure

Patients' residual tissue samples are collected

Electronic Health Record Review

Other

Medical records are reviewed

Primary outcomes

  1. Prospective and retrospective data collection on disease characterization, treatment, and outcomes

    Time frame: Up to 28 years

  2. Organization of clinical information

    Time frame: Up to 28 years

    Will 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.

  3. Creation of a single data repository to integrate clinical information and research findings

    Time frame: Up to 28 years

Secondary outcomes

  1. Collection and storage of human tumor samples for the establishment of a tumor bank

    Time frame: Up to 28 years

Study contacts

Contact information is provided by the study sponsor or research team.

Lisa Nathan

CONTACT

[email protected]

713-745-3837

Sponsors and collaborators

Lead sponsor

M.D. Anderson Cancer Center

Other

Registry information

Official study title

Data Collection for Patients With Low Grade Ovarian Carcinoma

Important dates

Study start
2006
Primary completion
2034
Study completion
2035
First posted
Jun 20, 2007
Registry last updated
Feb 13, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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