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Cancelled by the investigator A randomized controlled trial for high-dose Vitamin C in the treatment of severe and critical novel coronavirus pneumonia (COVID-19) patients

A randomized controlled trial for high-dose Vitamin C in the treatment of severe and critical novel coronavirus pneumonia (COVID-19) patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000030135
Enrollment
Unknown
Registered
2020-02-24
Start date
2020-02-25
Completion date
Unknown
Last updated
2020-03-16

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

Conditions

Novel Coronavirus Pneumonia (COVID-19)

Interventions

Experimental group:High-dose Vitamin C
Control group:Routine treatment

Sponsors

The Second Affiliated Hospital Of Xi'an Jiaotong University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Aged>=18 years old; 2. Diagnosed as severe and critical patients with novel coronavirus pneumonia; 3. Being treated in the ICU.

Exclusion criteria

Exclusion criteria: 1. Allergic to vitamin C; 2. Cardiogenic dyspnea; 3. Life expectancy<24h; 4. Pregnant and/or lactating female; 5. There is a state of tracheotomy or home oxygen therapy in the past; 6. Previously complicated with interstitial lung disease, malignant tumors,diffuse alveolar hemorrhage, diabetic ketoacidosis, or an active kidney stone; 7. Participating in other clinical trials; 8. Researchers believe patients are not suitable for clinical trials for other reasons.

Design outcomes

Primary

MeasureTime frame
Ventilation-free days;mortality;

Secondary

MeasureTime frame
ICU length of stay;Chest CT;Routine blood test;C-reactive protein;Liver and renal function ;APACHE II scores;SOFA scores;Myocardial markers;Electrocardiogram;Adverse events;

Countries

China

Contacts

Public ContactGao Dengfeng

The Second Affiliated Hospital of Xi'an Jiaotong University

gaomedic@163.com+86 15091544672

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026