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Apheresis clinical trials

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NCT ID: NCT05191290 Completed - Anticoagulation Clinical Trials

Comparison of Biocompatibility of Plasmapheresis Procedures With Citrate and Heparin Anticoagulation

Start date: January 21, 2022
Phase: Phase 4
Study type: Interventional

Membrane plasmapheresis is one of the methods for treating immune diseases. Plasmapheresis removes autoantibodies and immune complexes, paraproteins, lipoproteins and reduces the concentration of cytokines. In membrane plasmapheresis, plasma is separated from blood cells by a highly permeable membrane. The filtered plasma is then discarded and replaced with replacement fluid. During the procedure, there is an activation of the coagulation system, because of the extracorporeal blood circulation. The anticoagulation during the procedure is therefore necessary.

NCT ID: NCT04846374 Completed - Apheresis Clinical Trials

Two is Better Than One: A Novel Venous Access System for Intermittent Apheresis

Start date: May 26, 2021
Phase:
Study type: Observational

Purpose: To describe a novel configuration of venous access for the performance of intermittent apheresis. Participants: 20 participants at UNC who were referred for change from a vortex port to a powerflow port. Procedures (methods): Placement of one of two configurations of the powerflow port and follow up visits between January 1, 2019 and December 31, 2023.

NCT ID: NCT00042627 Completed - Apheresis Clinical Trials

Prevalence and Risk of Cataracts in Granulocyte Donors

Start date: July 30, 2002
Phase: N/A
Study type: Observational

This study will investigate whether people who donate granulocytes (a type of white blood cell) by leukapheresis are at increased risk of developing cataracts (changes in the lens of the eye that can impair vision). Apheresis is a method of collecting large numbers of white blood cells. The procedure is similar to donating whole blood, but the collected blood is circulated through a cell separator machine, the white cells are extracted, and the rest of the blood is returned to the donor. Before the procedure, donors are given a steroid called dexamethasone. This drug temporarily increases the number of granulocytes circulating in the blood, thus allowing twice as many of these cells to be collected. Recently, one blood collection center reported greater numbers of cataracts in a small number of granulocyte donors who had received repeated doses of steroids for granulocyte mobilization. The donors were unaware that they had the cataracts, which were small and did not affect their vision. Although people who take high doses of steroids over a long period time are known to have an increased risk of cataracts, steroids given infrequently (and in the doses used for granulocyte donation) have not been associated with cataracts. This study will examine the eyes of granulocyte donors and of platelet donors. Platelets-blood components necessary for clotting-are also collected by pheresis, but donors are not given steroids before the procedure. The examination findings will be compared to see if there is a difference in the risk of cataract formation in the two groups. People 18 years of age and older who have donated granulocytes or platelets at the NIH Department of Transfusion Medicine four times or more since 1984 may be eligible for this study. Participants will undergo the following procedures: - Detailed medical history, including allergies, corticosteroid use, diabetes mellitus, and asthma - Detailed eye history, including cataracts, glaucoma, other eye diseases and infections, eye trauma, and corrective lenses - Detailed history of sun exposure - Eye examination, including measurement of visual acuity (eye chart test) and eye pressure, examination of the lens and retina. - Photographs of the eye using a special camera