Steroid Diabetes in Patients With Kidney Disease

NCT ID: NCT06161701

Last Updated: 2024-04-29

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Total Enrollment

300 participants

Study Classification

OBSERVATIONAL

Study Start Date

2024-01-10

Study Completion Date

2027-02-28

Brief Summary

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If steroid diabetes is not recognized in time, it will cause irreversible damage to the body. Nephropathy patients are more likely to have steroid diabetes ,the incidence rate up to 25%,due to hypoalbuminemia, high-dose hormone and other reasons, so they need to be closely followed up, identified and intervened in time.

Detailed Description

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1. Patients with nephrosis who had taken glucocorticoid for the first time were followed up, and those who had diabetes themselves were excluded.
2. Regularly follow up and record information on glucocorticoid medication, medications that have an impact on blood sugar, fasting blood sugar, 2-hour postprandial blood sugar, and glycated hemoglobin.
3. Notify relevant doctors of any cases of elevated blood sugar.
4. The total follow-up time is 1 year.

Conditions

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Nephrotic Syndrome

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Blood glucose management in patients with kidney disease after using glucocorticoids

Blood glucose monitoring for kidney disease patients after taking glucocorticoids

no intervention

Intervention Type OTHER

no intervention

Interventions

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no intervention

no intervention

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

1. Patients who need to use glucocorticoids due to the following diseases: nephrotic syndrome, Immunoglobulin A nephropathy, membranous nephropathy, Anti-neutrophil cytoplasmic antibodies (ANCA)-associated vasculitis (AAV), systemic lupus erythematosus;
2. Initial daily dose of glucocorticoids greater than or equal to 10mg of prednisolone;

Exclusion Criteria

1. Patients with diabetes;
2. Those who are unable to communicate through language;
3. Uremic patients;
4. Unable to perform blood glucose monitoring and follow-up as required;
5. Those who have used glucocorticoids within the past 3 months and have accumulated a dose of 10mg or more of prednisone;
6. Participated in other clinical studies。
Minimum Eligible Age

18 Years

Maximum Eligible Age

75 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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The Third Affiliated Hospital of Wenzhou Medical University

OTHER

Sponsor Role collaborator

The First People's Hospital of Xiaoshan District, Hangzhou City

UNKNOWN

Sponsor Role collaborator

The Fourth Affiliated Hospital of Zhejiang University School of Medicine

OTHER

Sponsor Role collaborator

Nanxun District People's Hospital of Huzhou City,China

UNKNOWN

Sponsor Role collaborator

Wenling Traditional Chinese Medicine Hospital

UNKNOWN

Sponsor Role collaborator

Affiliated Hospital of Jiaxing University

OTHER

Sponsor Role collaborator

Taizhou Hospital

OTHER

Sponsor Role collaborator

The First People's Hospital of Chun'an

UNKNOWN

Sponsor Role collaborator

Zhejiang Provincial People's Hospital

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Xiaolan Ye, master

Role: STUDY_DIRECTOR

Zhejiang Provincial People's Hospital

Locations

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Zhejiang provincial people's hospital

Hangzhou, Zhejiang, China

Site Status RECRUITING

Countries

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China

Central Contacts

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Xiaolan Ye, master

Role: CONTACT

+86-0571-85893117

Ping Huang, doctor

Role: CONTACT

+86-0571-85893117

Facility Contacts

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Xiaolan Ye, master

Role: primary

86-0571-85893117

Ping Huang, doctor

Role: backup

86-0571-85893117

Other Identifiers

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KT20220083

Identifier Type: -

Identifier Source: org_study_id

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