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Immunosuppression clinical trials

View clinical trials related to Immunosuppression.

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NCT ID: NCT04542954 Completed - Covid19 Clinical Trials

Optimized Management of Covid-19 Positive Kidney Transplant Recipients: Single Center Experience From the Middle East

OMC-KTR
Start date: March 1, 2020
Phase:
Study type: Observational [Patient Registry]

Methods: Out of 2000 kidney transplant recipients in our center in Kuwait, collecting data was started for all COVID-19-positive kidney transplant recipients till August 2020. Clinical features, management details and both patient and graft outcomes were reported.

NCT ID: NCT04324853 Completed - Clinical trials for Vitamin D Deficiency

Helminth Infection During Pregnancy on Vitamin D Regulation: HELMVIT Study

HELMVIT
Start date: January 28, 2019
Phase:
Study type: Observational

Purpose: To examine whether helminth infection during pregnancy alters Vitamin-D-metabolism and reactivity of the child's immune system Hypothesis: Helminth infection during pregnancy is associated with altered Vitamin D levels and Vitamin D receptor expression in the placenta and modified immune reactivity in the infant.

NCT ID: NCT04177095 Completed - Immunosuppression Clinical Trials

Immune Monitoring to Facilitate Belatacept Monotherapy

Start date: February 11, 2020
Phase: Phase 4
Study type: Interventional

- To determine the utility of novel blood-based immune monitoring tools (Allosure and Trugraf) to facilitate belatacept monotherapy. - To determine the percent of belatacept-treated renal transplant patients that can be safely converted to belatacept monotherapy.

NCT ID: NCT04170309 Completed - Renal Insufficiency Clinical Trials

Collection of Data of Ceftobiprole Treated Patients: Comparison of Patients With and Without Certain Diseases

RETRACE
Start date: March 30, 2020
Phase:
Study type: Observational

In this observational study, data from patients treated with the antibiotic ceftobiprole in the past will be collected. The sponsor of the study is Correvio International Sárl, based in Switzerland. Correvio has committed to the health authorities to obtain further information on possible side effects especially in patients suffering from impaired liver or renal function or immune system deficiency and compare these effects to the ones observed in patients without these health problems. Patient data are collected from historic patient charts, patients will not be treated for the purpose of this data collection. All efforts are being made to capture the data of all patients who meet the inclusion criteria and have received at least one dose of ceftobiprole since this drug was first prescribed at the site.

NCT ID: NCT04041219 Completed - Immunosuppression Clinical Trials

Use of Sublingual Tacrolimus in Adult Blood and Marrow Transplant Patients

Start date: June 17, 2019
Phase: Phase 4
Study type: Interventional

Researchers are trying to learn more about using sublingual (absorption under the tongue) tacrolimus in blood and marrow transplant patients.

NCT ID: NCT03751332 Completed - Renal Failure Clinical Trials

The Vienna Prograf and Endothelial Progenitor Cell Extension Study

PEP-X
Start date: March 2008
Phase: Phase 4
Study type: Interventional

Conversion of renal transplant recipients from either tacrolimus or cyclosporin A to tacrolimus modified release to investigate the effects of the MDR1/CYP450 genotype on the trough blood levels of tacrolimus with modified galenic (tacrolimus MR4; Advagraf®).

NCT ID: NCT03316274 Completed - HIV/AIDS Clinical Trials

Intra-lesional Nivolumab Therapy for Limited Cutaneous Kaposi Sarcoma

Start date: May 7, 2018
Phase: Early Phase 1
Study type: Interventional

There is no clear treatment for patients with limited cutaneous Kaposi sarcoma (KS). Radiation and injection of vinblastine both have side effects that may not be acceptable. Nivolumab has been used to treat more extensive KS when given intravenously. This is, to the investigators' knowledge, the first trial to see if nivolumab can be used as treatment in the form of an injection into KS lesion.

NCT ID: NCT03139565 Completed - Influenza Clinical Trials

High Dose vs. Standard Influenza Vaccine in Adult SOT

Start date: October 2016
Phase: Phase 3
Study type: Interventional

The study will test whether a high dose influenza vaccination results in improved immunogenicity in adult SOT recipients as compared to standard vaccine. This will be a single center prospective observer-blind randomized controlled trial conducted at the Toronto General Hospital Multi-Organ Transplant Unit, University Health Network, Toronto, Ontario, Canada.

NCT ID: NCT03117192 Completed - Immunosuppression Clinical Trials

Zinc Supplementation on Cellular Immunity in Thalassemia Major

Start date: September 1, 2013
Phase: Phase 4
Study type: Interventional

Randomized controlled trial was conducted in post-splenectomy patients aged >12 years. Subjects are randomly assigned to two groups (zinc and placebo). 1.5 mg/kg/day (max 50 mg/day) of Zinc is administered.

NCT ID: NCT02978300 Completed - Clinical trials for Acute Respiratory Failure

HFNC Alone or Associated With NIV for Immunocompromised Patients Admitted to ICU for Acute Respiratory Failure

FLORALI-IM
Start date: January 21, 2017
Phase: N/A
Study type: Interventional

Acute respiratory failure is the leading cause of ICU admission of immunocompromized patients. In this subgroup of patients, the need for intubation and invasive mechanical ventilation occurs in about 50% of cases and is associated with very a high mortality rate, reaching 70% of cases. Therefore, noninvasive oxygenation strategies have been developed to avoid intubation. More than 15 years ago, 2 trials have suggested that NIV could decrease intubation and mortality rates of immunocompromized patients as compared to standard oxygen through a mask. However these results have not been confirmed in a recent large trial. HFNC is a recent and well-tolerated oxygenation technique. In a recent trial, HFNC alone could decrease mortality and intubation rates in patients with ARF as compared to NIV. Similar findings have been reported in a post-hoc analysis on immunocompromized patients excluding those with profound neutropenia. Likewise in a retrospective monocentric cohort of immunocompromized patients, we reported better outcomes with HFNC than with NIV.