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Detecting Abnormal Blood Clotting in Patients With Metastatic Cancer Undergoing Surgery

Primary Purpose

Thromboembolism, Unspecified Adult Solid Tumor, Protocol Specific

Status
Completed
Phase
Locations
United States
Study Type
Observational
Intervention
coagulation study
immunoenzyme technique
laboratory biomarker analysis
physiologic testing
study of high risk factors
Sponsored by
National Cancer Institute (NCI)
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an observational trial for Thromboembolism focused on measuring thromboembolism, unspecified adult solid tumor, protocol specific

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

DISEASE CHARACTERISTICS: Patients meeting the following criteria: Diagnosis of metastatic carcinoma Must be enrolled in 1 of the following surgical protocols: NCI-99-C-0123 NCI-00-C-0069 NCI-03-C-0085 NCI-03-C-0212 Healthy control participant* meeting the following criteria: No anemia or thrombocytopenia No history of venous thromboembolism (deep vein thrombosis, pulmonary emboli) No history of coronary artery disease or stroke No chronic inflammatory disease No diabetes mellitus Have not smoked tobacco within the past 6 months NOTE: * Selected on the basis of gender and age to match the patients as they are accrued PATIENT CHARACTERISTICS: No symptomatic infections or other acute illness within the past 14 days PRIOR CONCURRENT THERAPY: At least 3 days since prior drugs known to inhibit platelet function At least 7 days since prior acetylsalicylic acid No concurrent estrogen contraceptives or hormone replacement therapy No concurrent anticoagulants

Sites / Locations

  • National Institutes of Health Clinical Center, 9000 Rockville Pike

Outcomes

Primary Outcome Measures

Incidence of hypercoagulability

Secondary Outcome Measures

Comparison of the results of whole blood thrombin generation assay tests in patients who develop venous thromboembolism with those who do not

Full Information

First Posted
November 11, 2004
Last Updated
May 9, 2009
Sponsor
National Cancer Institute (NCI)
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1. Study Identification

Unique Protocol Identification Number
NCT00096590
Brief Title
Detecting Abnormal Blood Clotting in Patients With Metastatic Cancer Undergoing Surgery
Official Title
Evaluation of a Novel Blood Test Hypercoagulability in Surgical Patients With Metastatic Carcinoma: A Pilot Study
Study Type
Observational

2. Study Status

Record Verification Date
June 2007
Overall Recruitment Status
Completed
Study Start Date
November 2004 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
undefined (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
National Cancer Institute (NCI)

4. Oversight

5. Study Description

Brief Summary
RATIONALE: A test that detects abnormal blood clotting in patients with cancer may help doctors plan cancer surgery. PURPOSE: This laboratory study is looking at a new blood test to detect abnormal clotting in patients with metastatic cancer undergoing surgery.
Detailed Description
OBJECTIVES: Primary Determine whether whole blood thrombin generation assay (WBTGA) detects hypercoagulability in patients with metastatic carcinoma compared with a healthy control group. Determine whether results of the WBTGA will change as a result of major surgery performed on patients with metastatic carcinoma. Establish a reference interval for the WBTGA using healthy controls. Secondary Compare a battery of plasma components known to affect or reflect coagulant or fibrinolytic reactions in patients with metastatic carcinoma vs healthy controls. Establish reference intervals for this battery of tests using healthy controls. Determine how major surgery in cancer patients affects this battery of factors. Identify changes in these factors that correlate with changes in the WBTGA. Compare the results of WBTGA tests in patients who develop venous thromboembolism (VTE) with those who do not. OUTLINE: This is a pilot study. Blood samples of patients are collected on day -7 and day 1 after surgery. Blood samples of healthy controls are collected once. After collection, blood samples are analyzed for hypercoagulability by whole blood thrombin generation assay. Routine blood tests are performed, as are immunoenzyme techniques for antigenic tissue plasminogen activator and its inhibitor, thrombin-antithrombin complexes, tissue factor, factor VIIa, D-dimer, and glycocalicin. PROJECTED ACCRUAL: A total of 30 patients and 30 healthy controls will be accrued for this study.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Thromboembolism, Unspecified Adult Solid Tumor, Protocol Specific
Keywords
thromboembolism, unspecified adult solid tumor, protocol specific

7. Study Design

Enrollment
60 (Anticipated)

8. Arms, Groups, and Interventions

Intervention Type
Other
Intervention Name(s)
coagulation study
Intervention Type
Other
Intervention Name(s)
immunoenzyme technique
Intervention Type
Other
Intervention Name(s)
laboratory biomarker analysis
Intervention Type
Other
Intervention Name(s)
physiologic testing
Intervention Type
Procedure
Intervention Name(s)
study of high risk factors
Primary Outcome Measure Information:
Title
Incidence of hypercoagulability
Secondary Outcome Measure Information:
Title
Comparison of the results of whole blood thrombin generation assay tests in patients who develop venous thromboembolism with those who do not

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
DISEASE CHARACTERISTICS: Patients meeting the following criteria: Diagnosis of metastatic carcinoma Must be enrolled in 1 of the following surgical protocols: NCI-99-C-0123 NCI-00-C-0069 NCI-03-C-0085 NCI-03-C-0212 Healthy control participant* meeting the following criteria: No anemia or thrombocytopenia No history of venous thromboembolism (deep vein thrombosis, pulmonary emboli) No history of coronary artery disease or stroke No chronic inflammatory disease No diabetes mellitus Have not smoked tobacco within the past 6 months NOTE: * Selected on the basis of gender and age to match the patients as they are accrued PATIENT CHARACTERISTICS: No symptomatic infections or other acute illness within the past 14 days PRIOR CONCURRENT THERAPY: At least 3 days since prior drugs known to inhibit platelet function At least 7 days since prior acetylsalicylic acid No concurrent estrogen contraceptives or hormone replacement therapy No concurrent anticoagulants
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
McDonald K. Horne, MD
Organizational Affiliation
National Cancer Institute (NCI)
Official's Role
Principal Investigator
Facility Information:
Facility Name
National Institutes of Health Clinical Center, 9000 Rockville Pike
City
Bethesda
State/Province
Maryland
ZIP/Postal Code
20892
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
17570509
Citation
Horne MK 3rd, Merryman PK, Cullinane AM, Nghiem K, Alexander HR. The impact of major surgery on blood coagulation factors and thrombin generation. Am J Hematol. 2007 Sep;82(9):815-20. doi: 10.1002/ajh.20963.
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Detecting Abnormal Blood Clotting in Patients With Metastatic Cancer Undergoing Surgery

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