Skip to content

Nicotinamide-based Supportive Therapy in Lymphopenia for Patients With COVID-19

Efficiency and Safety of Nicotinamide-based Supportive Therapy in Lymphopenia for Patients With COVID-19: A Randomized Clinical Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04910230
Enrollment
24
Registered
2021-06-02
Start date
2020-03-01
Completion date
2020-04-02
Last updated
2021-11-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Covid19, Lymphopenia

Keywords

nicotinamide, COVID19, lymphopenia

Brief summary

The mechanism of peripheral blood lymphocyte decline in COVID-19 patients is not yet clear. However, one theory demonstrated that in the whole progression of COVID-19, the extensive activation of poly-ADP-ribose polymerase (PARP) may reduce the cellular NAD+ and dampen the adaptive immune system. So investigators presume that replenishing the NAD+ using nicotinamide as the precursor may improve the lymphocyte counts and boost the adaptive immune system. As a result, the study using nicotinamide as a kind of supportive therapy provide further evidence of their efficiency and safety in treating lymphopenia in patients with COVID-19.

Interventions

DRUGnicotinamide

In addition to usual care, the treatment group was given 500mg nicotinamide daily, divided into 5 doses

Sponsors

Qiang Hu
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
DOUBLE (Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

* the patients diagnosed as the common or severe cases of COVID-19 * aged 18-85 * the absolute lymphocyte counts below the normal value (\<1.1-3.2×109/L)

Exclusion criteria

* the patients who are diagnosed as critically ill cases or participating in other clinical trials * women who are pregnant or lactating * ALT/AST \> 5 times upper limit of normal (ULN), neutrophils counts \< 0.5×109/L, platelets counts\< 50×109/L * patients diagnosed with rheumatoid immune-related diseases * patients who take long-term oral anti-rejection drugs or immunomodulatory drugs * hypersensitive reaction to nicotinamide or any auxiliary materials * patients with active tuberculosis or combined with bacterial and fungal infections * patients undergoing organ transplant * patients with mental disorders.

Design outcomes

Primary

MeasureTime frameDescription
changes in absolute lymphocyte countsbefore and 48 hours after interventionthe changes in absolute lymphocyte counts (\*10\^9/L) in before and 48 hours after treatment

Secondary

MeasureTime frameDescription
the death in hospitalbefore and 48 hours after interventionthe rate of death in hospital (%)
the composite endpoint of aggravationbefore and 48 hours after interventionthe rate of composite endpoint of aggravation(%) , according to upgraded oxygen therapy, improvement of nursing level, and ward rounds of superior physicians for changes of conditions using the time to event principle. The upgraded oxygen therapy, improvement of nursing level, and ward rounds of superior physicians for changes of conditions would be combined to the composite endpoint in percentage (%). The upgraded oxygen therapy was defined as upgrading of ge neral high-volume oxygen intake from oxygen intake, ventilator using from high-volume oxygen intake or transference to intensive care unit from ventilator using.

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026