Skip to content

Effect of Amubarvimab/Romlusevimab (BRII-196/198) administration on prognosis in patients post SARS-CoV-2 infection: a follow-up cohort study

Effect of Amubarvimab/Romlusevimab (BRII-196/198) administration on prognosis in patients post SARS-CoV-2 infection: a follow-up cohort study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400080130
Enrollment
Unknown
Registered
2024-01-22
Start date
2024-01-22
Completion date
Unknown
Last updated
2024-01-28

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

Conditions

COVID-19

Interventions

Control group:N/A
Medication group:N/A

Sponsors

The First Affiliated Hospital of Guangzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Exposure group: 1,Patients with SARS-CoV-2 infection admitted to hospital from 1 January 2021 to 31 May 2023. 2,Received Amubarvimab/Romlusevimab (BRII-196/198) administration during hospitalisation after diagnosis of SARS-CoV-2 infection. 3,Age = 18 years. Control group: 1,Patients with SARS-CoV-2 infection admitted to hospital from 1 January 2021 to 31 May 2023. 2,Never had an administration of Amubarvimab/Romlusevimab (BRII-196/198). 3,Age = 18 years.

Exclusion criteria

Exclusion criteria: 1,Refusal to participate in this study. 2,Unable to complete the necessary questionnaires. 3,COVID-19 Vaccination history unknown and lack of clinical information. 4,Death before follow-up.

Design outcomes

Primary

MeasureTime frame
Neutralizing activity of serum;

Secondary

MeasureTime frame
Absolute lymphocyte subsets count;Interleukin-6;COVID-19 IgM and IgG;mMRC dyspnea score;Lung function;

Countries

China

Contacts

Public ContactYonghao Xu

The First Affiliated Hospital of Guangzhou Medical University

dryonghao@163.com+86 138 2840 9707

Outcome results

None listed

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