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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05691179
Other study ID # 2022-P2-429-01
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date December 10, 2022
Est. completion date May 31, 2023

Study information

Verified date February 2023
Source Beijing Friendship Hospital
Contact Zongli Diao, Dr.
Phone 86-10-63138579
Email diaozl@ccmu.edu.cn
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

Infection is one of common risk factors for relapsing of idiopathic membranous nephropathy (IMN). However, it is still unclear wheather COVID-19 infection can induce the relapsing of IMN. Herein, in this prospective, multi-center, cohort study, the investigator enrolled the IMN patients with COVID-19 infection. All subjects will be followed for three months with four visits at 1, 2 and 3 months. Then the investigator will compare the rate of replase of IMN in the two groups to evaluate the association of COVID-19 infection and replapse of IMN.


Recruitment information / eligibility

Status Recruiting
Enrollment 130
Est. completion date May 31, 2023
Est. primary completion date May 31, 2023
Accepts healthy volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: 1. the status of nephrotic syndrome is complete remmision or partial remmision; 2. estimated glomerular filtration rate (eGFR according to the CKD-EPI formula) =60 mL/min per 1.73 m2; 3. patients with a moderate risk of IMN. Exclusion Criteria: 1. secondary causes of MN; 2. the labarotary data two months before enrolement is absent.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
China Beijing Friedship Hospital Beijing Beijing
China Beijing Liangxiang Hospital Beijing Beijing
China Beijing Pinggu Hospital Beijing Beijing

Sponsors (3)

Lead Sponsor Collaborator
Beijing Friendship Hospital Beijing Fangshan District Liangxiang Hospital, Beijing Pinggu District Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary primary outcome relaspe of nephrotic syndrome: proteinuria<0.3g/d, serum albumin>30g/l, serum creatitine below 111 µmol/l 3 months
Secondary secondary outcome relaspe of nephrotic syndrome: proteinuria<3.5g/d (decreased over 50% of baseline), serum albumin>30g/l, steady serum creatitine (fluctuated less than 20% of baseline), meet the above criteria over 2 times 0.5, 1, and 2 months
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