MUMC+
Maastricht, Limburg, Netherlands
NCT Number: NCT03964688
In the study the investigators will randomize patients that receive an autologous stem cell transplantation for myeloma or lymphoma for treatment with vitamin C or placebo during 6 weeks. Primary endpoint will be immune recovery.
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Notify Me18 year and older
All sexes
Interventional
Phase 2
Maastricht, Limburg, Netherlands
Rationale: Recent studies showed that ascorbic acid (AA) stimulates proliferation and maturation of T lymphocytes and natural killer (NK) cells. Chemotherapy results in depletion of those cells and thereby an increased infection rate. A pilot study showed low levels of AA in the plasma of several patients after chemotherapy followed by autologous stem cell transplantation for hematological malignancies. AA supplementation could be beneficial to the recovery of the immune system in these patients.
Objective: The aim of this study is to examine the effect of vitamin C supplementation on immune recovery in patients with autologous stem cell transplantation. The aim of the run-in phase of the study is to examine the effect of intravenous vitamin C supplementation on plasma concentrations of vitamin C in patients with autologous stem cell transplantation at day 14 in order to be sure that in the intervention study accurate AA plasma levels will be present.
Study design: run-in phase, followed by randomized controlled trial Study population: All participants will be adults (minimally 18 years old) that are planed to receive an autologous stem cell transplantation for multiple myeloma or lymphoma and are recruited at the MUMC+. In total there will be 3 expected (run-in phase) + 44 (randomized controlled trial) participants.
Main study parameters/endpoints: Primary endpoints will be AA plasma level on day 14 (run-in phase) and the day of neutrophil recovery after stem cell transplantation (randomized-controlled phase). Secondary endpoints will be AA leukocyte levels, infection rate, duration of hospital stay, side effects of chemotherapy, overall survival, coagulation parameters, platelet reactivity, fibrinolysis and quality of life.
Nature and extent of the burden and risks associated with participation, benefit and group relatedness:
AA supplementation could be beneficial for the immune recovery in the participants of this study. The risks associated with participation in this study are low. Vitamin C supplementation is safe and hardly has any documented side effects.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
vitamin C intravenous during hospitalization, after oral, total 6 weeks.
Other names: ascorbic acid
placebo intravenous during hospitalization, after oral, total 6 weeks
Other names: placebo
Time frame: day 14-28
the day of repopulation (return of neutrophil to at least 0.5 × 109/l) after autologous stem cell transplantation.
Time frame: day 14
AA plasma levels
Time frame: day 14
AA leukocyte levels
Time frame: day 1-28
fever and infections during hospitalization
Time frame: dag 1-28
number of days patients are admitted in our hospital
Time frame: day 1-28
Amount of days admitted patients have a fever
Time frame: day1-28
number of bloodstream infections of admitted patients
Time frame: Day 0, day 14, day 42
quality of live questionaire
Time frame: 3 months
overall survival at 3 months
Time frame: 3 months
relapse rate at 3 months
Time frame: dau 1-28
use of antibiotics during hospitalization
Time frame: day 10
platelet reactivity tests
Time frame: day 10
ROS production platelets
Time frame: day 10
platelet mitochondrial function test
Time frame: day 1-28
number and severity of bleeding episodes during admission
Maastricht University Medical Center
Other
Randomized Controlled Trial on the Effect of Vitamin C Supplementation in Autologous Stem Cell Transplantations
Acronym: VICAST
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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