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Clinical study for prevention and treatment of digestive tract lesions caused by novel coronavirus pneumonia (COVID-19)

Clinical study for prevention and treatment of digestive tract lesions caused by novel coronavirus pneumonia (COVID-19)

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000031454
Enrollment
Unknown
Registered
2020-04-01
Start date
2020-01-25
Completion date
Unknown
Last updated
2020-04-06

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:Rabeprazole plus chloroquine
control group :Lopinavir + rabeprazole

Sponsors

Infection prevention and treatment center of The Fifth Affiliated Hospital of Sun Yat-Sen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18 to 75 years old; 2. mild or normal patients; 3. not using chloroquine phosphate, lopinavir other than other antiviral drugs; 4. under the gastroscope, there was mucosal damage and pathological biopsy of 2019-ncov nucleic acid positive; 5. confirmed cases meeting all the following criteria (the 5th edition of the medical guidelines): (1) epidemiological history; (2) Clinical manifestations (in accordance with any 2 of the following): fever; In the early stage of the disease, the total number of white blood cells was normal or decreased, or the lymphocyte count was decreased. In the early stage of chest imaging, multiple small plaques and stromal changes were observed, especially in the lung. Then, it developed into multiple ground-glass shadows and infiltrating shadows in both lungs. In severe cases, lung consolidation may occur, and pleural effusion is rare; (3) Confirmed: the suspected case has one of the following etiological evidence: respiratory or blood specimens were tested positive for novel coronavirus nucleic acid by real-time fluorescent rt-pcr; Respiratory or blood specimen virus gene sequencing, and known novel coronavirus highly homologous.

Exclusion criteria

Exclusion criteria: 1. in pregnancy, breast-feeding female patients; 2. to determine the history of chloroquine phosphate, rabeprazole drug allergy patients; Patients suffering from diseases of the blood system; 3. patients suffering from chronic liver and kidney diseases and reaching the terminal stage; 4. Serious heart, lung dysfunction and mental illness; 5. Patients with known retinal diseases, hearing loss or hearing loss; 6. Patients who have to take digitalis drugs for existing underlying diseases; 7. Merger of other digestive tract diseases; 8. Combine ribavirin; 9. Involved in other processing clinical drug trials.

Design outcomes

Primary

MeasureTime frame
2019-ncov nucleic acid yin rate;Blood 2019-ncov nucleic acid positive;Positive 2019-ncov nucleic acid in feces;Nasopharyngeal swab positive for 2019-ncov nucleic acid;

Countries

China

Contacts

Public ContactXiao Fei

The Fifth Affiliated Hospital of Sun Yat-Sen University

xiaof35@sysu.edu.cn+86 13380600018

Outcome results

None listed

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