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Completed

NCT Number: NCT03964688

Effect of Vitamin C in Autologous Stem Cell Transplantations

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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Key information

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 18 years or older
  • written informed consent
  • diagnosis of malignant lymphoma or multiple myeloma
  • require chemotherapy plus autologous stem cell transplantation as standard of care for the disease at that stage
  • central venous catheter in place or planned

Exclusion criteria

  • inability to understand the nature and extent of the trial and the procedures required
  • history of kidney stones
  • kidney failure requiring dialysis or eGFR <30 mL/min. (CDK-EPI formula)
  • history of G6PD deficiency
  • life expectancy < 1 month
  • use of immunosuppressive medication other than chemotherapy and corticosteroids

Treatment and study plan

Vitamin C

Drug

vitamin C intravenous during hospitalization, after oral, total 6 weeks.

Other names: ascorbic acid

Placebos

Drug

placebo intravenous during hospitalization, after oral, total 6 weeks

Other names: placebo

Primary outcomes

  1. immune recovery

    Time frame: day 14-28

    the day of repopulation (return of neutrophil to at least 0.5 × 109/l) after autologous stem cell transplantation.

Secondary outcomes

  1. AA plasma levels

    Time frame: day 14

    AA plasma levels

  2. AA leukocyte levels

    Time frame: day 14

    AA leukocyte levels

  3. Incidence of infections/ neutropenic fever

    Time frame: day 1-28

    fever and infections during hospitalization

  4. Days of hospitalization

    Time frame: dag 1-28

    number of days patients are admitted in our hospital

  5. Days with fever (≥ 38.5° C)

    Time frame: day 1-28

    Amount of days admitted patients have a fever

  6. Incidence of bloodstream infections

    Time frame: day1-28

    number of bloodstream infections of admitted patients

  7. Quality of life according to the EORTC QLQ-C30

    Time frame: Day 0, day 14, day 42

    quality of live questionaire

  8. Overall survival (3 months)

    Time frame: 3 months

    overall survival at 3 months

  9. Relapse rates (3 months)

    Time frame: 3 months

    relapse rate at 3 months

  10. Use of systemic antimicrobial agents (incidence and duration)

    Time frame: dau 1-28

    use of antibiotics during hospitalization

  11. platelet reactivity

    Time frame: day 10

    platelet reactivity tests

  12. ROS production

    Time frame: day 10

    ROS production platelets

  13. platelet mitochondrial dysfunction

    Time frame: day 10

    platelet mitochondrial function test

  14. number and severity of bleeding episodes during admission

    Time frame: day 1-28

    number and severity of bleeding episodes during admission

Sponsors and collaborators

Lead sponsor

Maastricht University Medical Center

Other

Registry information

Official study title

Randomized Controlled Trial on the Effect of Vitamin C Supplementation in Autologous Stem Cell Transplantations

Acronym: VICAST

Important dates

Study start
2019
Primary completion
2022
Study completion
2022
First posted
May 28, 2019
Registry last updated
Apr 20, 2022

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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