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NCT05926076 Clinical Trial

COVID-19 Infection

COVID-19 Clinical Trial

Official title:
Comparative Study of COVID-19 Infection in Renal Transplant Recipients and Non Transplant Recipients

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT05926076
Other study ID # 2023-036-02
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date July 25, 2023
Est. completion date July 30, 2023

Study information
Verified date June 2023
Source Tianjin First Central Hospital
Contact Yingxin Fu, MD
Email fuyingxin@vip.163.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Post-transplant patients with COVID-19 infection who attended Shenzhen No. 3 Hospital from December 2022 to February 2023, and enrolled the general population with COVID-19 infection who were hospitalized during the same period, matched by age and gender.

Description:

Data collection：Age, BMI, underlying comorbidities and other basic information were collected retrospectively from the two groups. The medical records were used to collect information about the patients' new coronavirus infection, such as the time of onset of symptoms, time of diagnosis, time of conversion and common symptoms such as fever, cough, nasal congestion and runny nose, muscle aches and pains.To compare the differences of the diagnosis and treatment of KTRs and the general population infected with Omicron

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 610
Est. completion date July 30, 2023
Est. primary completion date July 30, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: Confirmed novel coronavirus infection between December 2022 to February 2023, Exclusion Criteria: Age less than 18; failure of the transplanted kidney before the new coronavirus infection; exclusion of oral immunosuppressed and other types of organ transplant recipients from the non-renal transplant population

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Treatment plan
Patients with different diagnoses will get different treatment options

Locations
Country Name City State
China yingxin Fu Shenzhen Guangdong

Sponsors (2)
Lead Sponsor Collaborator
Tianjin First Central Hospital Shenzhen Third People's Hospital

Country where clinical trial is conducted

China, 

Outcome
Type Measure Description Time frame Safety issue
Primary ICU admission or death patients have ICU admission or death through study completion, an average of 1 month
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