Vitamin C Infusion for the Treatment of Severe 2019-nCoV Infected Pneumonia
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|ClinicalTrials.gov Identifier: NCT04264533|
Recruitment Status : Not yet recruiting
First Posted : February 11, 2020
Last Update Posted : February 11, 2020
2019 new coronavirus (2019-nCoV) infected pneumonia, namely severe acute respiratory infection (SARI) has caused global concern and emergency. There is a lack of effective targeted antiviral drugs, and symptomatic supportive treatment is still the current main treatment for SARI.
Vitamin C is significant to human body and plays a role in reducing inflammatory response and preventing common cold. In addtion, a few studies have shown that vitamin C deficiency is related to the increased risk and severity of influenza infections.
We hypothize that Vitamin C infusion can help improve the prognosis of patients with SARI. Therefore, it is necessary to study the clinical efficacy and safety of vitamin C for the clinical management of SARI through randomized controlled trials during the current epidemic of SARI.
|Condition or disease||Intervention/treatment||Phase|
|Vitamin C Pneumonia, Viral Pneumonia, Ventilator-Associated||Drug: Vit C Drug: Water for infusion||Phase 2|
At the end of 2019, patients with unexplained pneumonia appeared in Wuhan, China. At 21:00 on January 7, 2020, a new coronavirus was detected in the laboratory, and the detection of pathogenic nucleic acids was completed at 20:00 on January 10. Subsequently, the World Health Organization officially named the new coronavirus that caused the pneumonia epidemic in Wuhan as 2019 new coronavirus (2019-nCoV), and the pneumonia was named severe acute respiratory infection (SARI). Up to February 4, 2020, over 20000 cases have been diagnosed in China, 406 of which have died, and 154 cases have been discovered in other countries around the world. Most of the deaths were elderly patients or patients with severe underlying diseases. SARI has caused global concern and emergency.
Statistics of the 41 patients with SARI published in JAMA initially showed that 13 patients were transferred into the ICU, of which 11 (85%) had ARDS and 3 (23%) had shock. Of these, 10 (77%) required mechanical ventilation support, and 2 (15%) required ECMO support. Of the above 13 patients, 5 (38%) eventually died and 7 (38%) were transferred out of the ICU. Viral pneumonia is a dangerous condition with a poor clinical prognosis. For most viral infections, there is a lack of effective targeted antiviral drugs, and symptomatic supportive treatment is still the current main treatment.
Vitamin C, also known as ascorbic acid, has antioxidant properties. When sepsis happens, the cytokine surge caused by sepsis is activated, and neutrophils in the lungs accumulate in the lungs, destroying alveolar capillaries. Early clinical studies have shown that vitamin C can effectively prevent this process. In addition, vitamin C can help to eliminate alveolar fluid by preventing the activation and accumulation of neutrophils, and reducing alveolar epithelial water channel damage. At the same time, vitamin C can prevent the formation of neutrophil extracellular traps, which is a biological event of vascular injury caused by neutrophil activation. Vitamins can effectively shorten the duration of the common cold. In extreme conditions (athletes, skiers, art workers, military exercises), it can effectively prevent the common cold. And whether vitamin C also has a certain protective effect on influenza patients, only few studies have shown that vitamin C deficiency is related to the increased risk and severity of influenza infections. In a controlled but non-randomized trial, 85% of the 252 students treated experienced a reduction in symptoms in the high-dose vitamin C group (1g / h at the beginning of symptoms for 6h, followed by 3 * 1g / day). Among patients with sepsis and ARDS, patients in the high-dose vitamin group did not show a better prognosis and other clinical outcomes. There are still some confounding factors in the existing research, and the conclusions are different.
Therefore, during the current epidemic of SARI, it is necessary to study the clinical efficacy and safety of vitamin C for viral pneumonia through randomized controlled trials.
|Study Type :||Interventional (Clinical Trial)|
|Estimated Enrollment :||140 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||Triple (Participant, Care Provider, Outcomes Assessor)|
|Official Title:||Vitamin C Infusion for the Treatment of Severe 2019-nCoV Infected Pneumonia: a Prospective Randomized Clinical Trial|
|Estimated Study Start Date :||February 10, 2020|
|Estimated Primary Completion Date :||September 30, 2020|
|Estimated Study Completion Date :||September 30, 2020|
Experimental: Vit C
24g Vitamin C+water for injection, total volume 50ml. 7ml/h; infusion pump.
Drug: Vit C
24g Vitamin C will be infused in the experimental group per day for 7 days by the infusion pump with a speed of 7ml/h.
Other Name: Vitamin C
Placebo Comparator: Water for injection
50ml water for injection. 7ml/h; infusion pump.
Drug: Water for infusion
50ml water for infusion will be infused in the placebo comparator group per day for 7 days by the infusion pump with a speed of 7ml/h.
- Ventilation-free days [ Time Frame: on the day 28 after enrollment ]days without ventilation support during 28 days after patients' enrollment
- 28-days mortality [ Time Frame: on the day 28 after enrollment ]wether the patient survives
- ICU length of stay [ Time Frame: on the day 28 after enrollment ]days of the patients staying in the ICU
- Demand for first aid measuments [ Time Frame: on the day 28 after enrollment ]t t the rate of CPR
- Vasopressor days [ Time Frame: on the day 28 after enrollment ]days of using vasopressors
- Respiratory indexes [ Time Frame: on the day 10 and 28 after enrollment ]P O2/Fi O2 which reflects patients' respiratory function
- Ventilator parameters [ Time Frame: on the day 10 and 28 after enrollment ]Ecmo or ventilator
- APACHE II scores [ Time Frame: on the day 10 after enrollment ]Acute Physiology and Chronic Health Evaluation
- SOFA scores [ Time Frame: on the day 10 after enrollment ]Sepsis-related Organ Failure Assessment
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04264533
|Contact: Zhiyong Peng, email@example.com|
|Zhongnan Hospital of Wuhan University|
|Wuhan, Hubei, China, 430000|
|Principal Investigator:||Zhiyong Peng, professor||Wuhan University|