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

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT01078350

Enrollment

Registered

2010-03-02

Start date

2004-05-31

Completion date

2015-12-04

Last updated

2017-11-20

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

Conditions

Hodgkin Disease, Lymphoma

Keywords

Lymphoma, Hodgkin Disease

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.

Interventions

PROCEDUREtumor tissue aspiration

PROCEDUREphlebotomy

Study design

Observational model

COHORT

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

No minimum to 21 Years

Healthy volunteers

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

* None.

Design outcomes

Primary

Measure	Time frame
Further analysis	at collection time

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026