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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03189108
Other study ID # 170100
Secondary ID 17-C-0100
Status Completed
Phase
First received
Last updated
Start date May 22, 2017
Est. completion date May 18, 2023

Study information

Verified date September 29, 2023
Source National Institutes of Health Clinical Center (CC)
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Background: Researchers want to study fluids and blood of people with cancer. The fluids are from the abdomen and around the lungs. Studying these might help researchers learn about the biology of cancer. This may lead to better ways to treat cancer. Objectives: To study the biology of cancer. Eligibility: Adults 18 and older with malignant solid tumors. Design: Participants will be screened with medical history, blood tests, and confirmation of diagnosis. Participants will have samples taken at regularly scheduled procedures. Fluids from the abdomen and/or lungs will be taken as part of the procedures. Blood will be taken separately. Participants may be asked to give more samples at future procedures. ...


Description:

Background: -Malignant ascites or pleural effusions are often seen in patients with solid tumor malignancies. -Malignant ascites is proinflammatory with many cytokines present and acts to promote tumor cell growth. -The cellular composition of malignant ascites consists of lymphocytes, macrophages and monocytes. -Serum monocytes and lymphocytes play a role in the native host anti-tumor immune mediated mechanisms. -A paracentesis or thoracentesis is often done for symptomatic relief from the malignant fluid collection. Primary Objective: -To obtain blood samples and ascites and pleural effusion samples from patients with solid tumor malignancies, with the intent of performing translational studies related to cancer. Eligibility: - Patients greater than or equal to 18 years of age. - Diagnosis of malignant solid tumor. - Patients must be able and willing to provide informed consent. Design: -We will collect approximately 200cc-5L ascites from patients that are undergoing a therapeutic paracentesis or thoracentesis. No thoracentesis or paracentesis will be performed solely for research purposes. -The fluid will be collected during the medical procedure and may be collected at more than one time point. -We will also collect 30ml of peripheral blood. This will be from patients who are being seen in follow up, consultation, or presenting for enrollment on a clinical trial.


Recruitment information / eligibility

Status Completed
Enrollment 22
Est. completion date May 18, 2023
Est. primary completion date May 18, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility - INCLUSION CRITERIA: - Participants greater than or equal to 18 years of age with histologically proven malignant solid tumors - Ability and willingness to provide informed consent to participation. - Participants with malignant solid tumors with a clinical indication for a thoracentesis or paracentesis. EXCLUSION CRITERIA: -Children < 18 years of age are not eligible.

Study Design


Locations

Country Name City State
United States National Institutes of Health Clinical Center Bethesda Maryland

Sponsors (1)

Lead Sponsor Collaborator
National Cancer Institute (NCI)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary To obtain blood samples, ascites and pleural effusion samples from patients with solid tumor malignancies, with the intent of performing translational studies related to cancer. Experimental - Translational study outcomes from the collection/analysis of blood samples; and ascites and pleural effusion samples from patients with solid tumor malignancies. Ongoing
Secondary Develop the malignant fluid as a culture model to replicate intraperitoneal growth of ovarian cancers. ongoing
Secondary Characterize malignant effusion composition through immunohistochemistry and flow cytometry. ongoing
Secondary Compare immune cell phenotype in ascites and blood from the patient. ongoing
Secondary Study in vivo characteristics of matched tumor cells and peripheral blood leukocytes from the same patient in xenograft models ongoing
Secondary Establish a bank of clinically annotated samples for translational science. ongoing
Secondary Compare selected matched sets of samples from the same patient to evaluate both for treatment response. ongoing
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