Molecular and Cellular Characterization of Skull Base Tumors

NCT ID: NCT03759717

Last Updated: 2025-09-22

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Total Enrollment

4000 participants

Study Classification

OBSERVATIONAL

Study Start Date

2018-10-03

Study Completion Date

2028-10-03

Brief Summary

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The purpose of the study is to analyze biological samples and genetic material for basic science research investigating the molecular and cellular characterization of skull base tumors.

Detailed Description

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The overall goal of this proposal is to determine new molecular and cellular features that define tumor subtypes that are clinically actionable, may drive important changes in patient management, and/or elucidate novel chemotherapeutic options. Skull base tumors are currently diagnosed based on histopathologic criteria, on which post-operative management is based. However, the investigators hypothesize that each tumor type (eg. chordoma or chondrosarcoma) will have molecular and/or cellular subcategories that will redefine how to categorize and diagnose patients, predict clinical outcome, and optimally design a patient-specific management strategy. In addition, we aim to catalogue changes that occur after treatment after surgical resection, chemotherapy, and/or radiation by comparing primary and recurrent tumors.

Conditions

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Skull Base Neoplasm Cellular Pathology

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Interventions

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Observation

Understanding the biology of skull base tumors will teach the investigators about the genesis and/or mechanisms of treatment resistance. The investigators hope to ultimately identify new targets which will add to the armamentarium by which to treat these tumors.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Diagnosis of a skull base tumor

Exclusion Criteria

* Insufficient tumor sample at time of resection
Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University of Pittsburgh

OTHER

Sponsor Role lead

Responsible Party

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Paul Gardner

Associate Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Paul Gardner, MD

Role: PRINCIPAL_INVESTIGATOR

Associate Professor

Locations

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University of Pittsburgh Medical Center

Pittsburgh, Pennsylvania, United States

Site Status RECRUITING

Countries

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United States

Central Contacts

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Benita Valappil, MPH

Role: CONTACT

412-864-1744

Facility Contacts

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Benita Valappil, MPH

Role: primary

412-864-1744

Other Identifiers

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STUDY19070185

Identifier Type: -

Identifier Source: org_study_id

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