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Clinical Trials/NCT01078350
NCT01078350CompletedNot Applicable

Consent for Obtaining Additional Tissue at the Time of a Diagnostic Biopsy

Stanford University1 site in 1 country93 target enrollmentStarted: May 2004Last updated:
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Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
93
Locations
1
Primary Endpoint
Further analysis
Study OverviewStudy DesignEligibility CriteriaOutcomesInvestigatorsSitesRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

This study is designed to collect tissue samples that may aid in the treatment and learning about various oncology diagnosis.

Detailed Description

The purpose of this study is to provide a mechanism to obtain tissue specimens to be used for experimental studies before the exact histologic diagnosis is known.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
— to 21 Years (Child, Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Subjects who are having a tissue procedure done as part of their standard oncology work-up will be eligible to be consented on this study.

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Further analysis

Time Frame: at collection time

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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Consent for Obtaining Additional Tissue at... | Clinical Trial