NCT00900471

Brief Summary

RATIONALE: Collecting and storing samples of tissue or blood from patients with cancer for study in the laboratory may help the study of cancer in the future PURPOSE: This research study is collecting and storing blood and tissue samples from patients with suspected solid tumors.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
20,000

participants targeted

Target at P75+ for all trials

Timeline
12mo left

Started Apr 2004

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress96%
Apr 2004May 2027

Study Start

First participant enrolled

April 1, 2004

Completed
5.1 years until next milestone

First Submitted

Initial submission to the registry

May 9, 2009

Completed
3 days until next milestone

First Posted

Study publicly available on registry

May 12, 2009

Completed
18 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 1, 2027

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

May 1, 2027

Last Updated

March 19, 2026

Status Verified

March 1, 2026

Enrollment Period

23.1 years

First QC Date

May 9, 2009

Last Update Submit

March 16, 2026

Conditions

Keywords

unspecified adult solid tumor, protocol specificunspecified childhood solid tumor, protocol specific

Outcome Measures

Primary Outcomes (1)

  • Tissue and cell repository for Wake Forest University Comprehensive Cancer Center investigators

    Day 1

Interventions

Eligibility Criteria

Age18 Years - 120 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Those with a clinically suspected solid tumor and scheduled for surgical resection and/or biopsy

You may qualify if:

  • Signed protocol specific informed consent prior to registration/randomization.
  • Clinically suspected solid tumor AND scheduled for surgical resection and/or biopsy

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Wake Forest University Comprehensive Cancer Center

Winston-Salem, North Carolina, 27157-1096, United States

RECRUITING

Biospecimen

Retention: SAMPLES WITH DNA

Solid Tumors Tissue

Study Officials

  • Edward A. Levine, MD

    Wake Forest University Health Sciences

    STUDY CHAIR

Central Study Contacts

Study Coordinator

CONTACT

Study Design

Study Type
observational
Observational Model
CASE ONLY
Time Perspective
OTHER
Target Duration
1 Day
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

May 9, 2009

First Posted

May 12, 2009

Study Start

April 1, 2004

Primary Completion (Estimated)

May 1, 2027

Study Completion (Estimated)

May 1, 2027

Last Updated

March 19, 2026

Record last verified: 2026-03

Locations