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Study on the changed characteristics of glycolipid and immune metabolism in patients with coronavirus disease 2019 (COVID-19) treated by Paxlovid

Study on the changed characteristics of glycolipid and immune metabolism in patients with coronavirus disease 2019 (COVID-19) treated by Paxlovid

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200059743
Enrollment
Unknown
Registered
2022-05-10
Start date
2022-05-08
Completion date
Unknown
Last updated
2024-03-25

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

Conditions

Covid-19

Interventions

Experimental group:Paxlovid
control group:No

Sponsors

Renji Hospital, Shanghai Jiaotong University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Test group: (1) Age: 18-75 years old; (2) Gender is not restricted; (3) Meet the diagnostic criteria of the Diagnosis and Treatment Program for Novel Coronavirus Pneumonia (Trial Ninth Edition); (4) Willing to use Paxlovid; (5) Patients with viral nucleic acid CT value > 35 if taking Paxlovid for less than 5 days; 2. Control group: (1) Age: 18-75 years old; (2) Gender is not restricted; (3) Meet the diagnostic criteria of the Diagnosis and Treatment Program for Novel Coronavirus Pneumonia (Trial Ninth Edition); (4) Unwilling to use Paxlovid; (5) Age, sex, body mass index, underlying disease and medication history were strictly matched with each subgroup of the clinical classification in the test group.

Exclusion criteria

Exclusion criteria: 1. Patients with advanced malignant tumor; 2. Kidney disease or severe renal insufficiency (renal function EGFR < 30ml/min/1.73m2); 3. Severe liver dysfunction (ALT/AST is more than 2.5 times the normal upper limit); 4. Other metabolic diseases other than diabetes, such as thyroid and adrenal diseases; 5. Rheumatoid immune diseases, etc. 6. Contraindications to the use of Nimatvir Tablets/Ritonavir Tablets; 7. Other circumstances that the researcher thinks are not suitable for study.

Design outcomes

Primary

MeasureTime frame
Fasting blood glucose;2 hours postprandial blood sugar;Glycated hemoglobin;Blood fat;

Secondary

MeasureTime frame
Covid-19 CT value;

Countries

China

Contacts

Public ContactJing Ma

Renji Hospital, Shanghai Jiaotong University School of Medicine

majing@renji.com+86 15800983436

Outcome results

None listed

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