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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT00471120
Other study ID # 13806-CC113
Secondary ID
Status Terminated
Phase N/A
First received May 7, 2007
Last updated August 3, 2015
Start date November 2006
Est. completion date February 2008

Study information

Verified date August 2015
Source CytoCore, Inc.
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

This study aims at developing an accurate, simple, and cost-effective method for screening and early detection of uterine cancers


Description:

The present study aims at developing an accurate, simple and cost-effective method for screening and early detection of uterine cancers in women using novel inventions and biotechnology methods for collection and assay of uterine cells. Results of P2X7 assays using tissues obtained from women with known uterine cancer and from women with histologically normal endometrium will be compared. These data will also serve as basis for future studies to test the predictive value of the method in population-based studies.


Recruitment information / eligibility

Status Terminated
Enrollment 20
Est. completion date February 2008
Est. primary completion date April 2007
Accepts healthy volunteers No
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria:

- women scheduled to undergo hysterectomy

- ages 18 years and older

Exclusion Criteria:

- pregnant women

- students or employees under the direct supervision on the investigators.

Study Design

Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Screening


Intervention

Other:
P2x7 assay
compare P2X7 assay to biopsy

Locations

Country Name City State
United States University Hospital CASE Medical Center Cleveland Ohio
United States University of Texas Dallas Texas
United States University of Texas Galveston Texas
United States University of Arkansas Little Rock Arkansas
United States Eastern Virginia Medical School Norfolk Virginia

Sponsors (1)

Lead Sponsor Collaborator
Dick Domanik

Country where clinical trial is conducted

United States, 

References & Publications (5)

Feng YH, Li X, Wang L, Zhou L, Gorodeski GI. A truncated P2X7 receptor variant (P2X7-j) endogenously expressed in cervical cancer cells antagonizes the full-length P2X7 receptor through hetero-oligomerization. J Biol Chem. 2006 Jun 23;281(25):17228-37. Epub 2006 Apr 18. — View Citation

Feng YH, Wang L, Wang Q, Li X, Zeng R, Gorodeski GI. ATP stimulates GRK-3 phosphorylation and beta-arrestin-2-dependent internalization of P2X7 receptor. Am J Physiol Cell Physiol. 2005 Jun;288(6):C1342-56. Epub 2005 Feb 23. — View Citation

Li X, Zhou L, Feng YH, Abdul-Karim FW, Gorodeski GI. The P2X7 receptor: a novel biomarker of uterine epithelial cancers. Cancer Epidemiol Biomarkers Prev. 2006 Oct;15(10):1906-13. — View Citation

Wang L, Feng YH, Gorodeski GI. Epidermal growth factor facilitates epinephrine inhibition of P2X7-receptor-mediated pore formation and apoptosis: a novel signaling network. Endocrinology. 2005 Jan;146(1):164-74. Epub 2004 Sep 30. — View Citation

Wang Q, Wang L, Feng YH, Li X, Zeng R, Gorodeski GI. P2X7 receptor-mediated apoptosis of human cervical epithelial cells. Am J Physiol Cell Physiol. 2004 Nov;287(5):C1349-58. Epub 2004 Jul 21. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary To determine the accuracy potential of the P2X7 (protein and mRNA levels) for the detection of uterine endometrial cancers in women. Upon review of the assays. No
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