- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06922370
The Osteoarticular Manifestations in Patients With Gitelman Syndrome (CPPD and more)
April 3, 2025 updated by: Second Affiliated Hospital, School of Medicine, Zhejiang University
Patients with clinically and genetically confirmed Gitelman Syndrome are screened for CPPD, and the clinical and radiographic manifestations are collected and analyzed.
Study Overview
Status
Recruiting
Intervention / Treatment
Detailed Description
Patients with clinically and genetically confirmed Gitelman Syndrome are screened for calcium pyrophosphate deposition, and the clinical data and radiographic manifestations are collected and analyzed to investigate the osteoarticular features in patients with Gitelman Syndrome.
Study Type
Observational
Enrollment (Estimated)
120
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Lijun Mou
- Phone Number: +86-0571-89713751
- Email: moulj511@zju.edu.cn
Study Locations
-
-
Zhejiang
-
Hangzhou, Zhejiang, China, 310005
- Recruiting
- The Second Affiliated Hospital, Zhejiang University School of Medicine
-
Contact:
- Ethics Committee of SAHZU
- Phone Number: +86-057187783969
- Email: keyanlunli_zheer@163.com
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
Patients clinically and genetically confirmed with Gitelman Syndrome
Description
Inclusion Criteria:
- Patients confirmed with Gitelman Syndrome
Exclusion Criteria:
- Patients with other confounding situations such as Bartter Syndrome, hyperparathyroidism
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Patients with Gitelman Syndrome
Patients with clinically and genetically confirmed Gitelman syndrome.
|
patients with gitelman syndrome evaluated with conventional radiograph or computed tomography
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The presence of chondrocalcinosis
Time Frame: From the enrollment to the performance of the CPPD screen
|
The presence of chondrocalcinosis on conventional radiograph or computed tomography in patients with Gitelman Syndrome
|
From the enrollment to the performance of the CPPD screen
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
November 1, 2021
Primary Completion (Estimated)
November 1, 2025
Study Completion (Estimated)
December 1, 2025
Study Registration Dates
First Submitted
April 3, 2025
First Submitted That Met QC Criteria
April 3, 2025
First Posted (Actual)
April 10, 2025
Study Record Updates
Last Update Posted (Actual)
April 10, 2025
Last Update Submitted That Met QC Criteria
April 3, 2025
Last Verified
March 1, 2025
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Crystal Arthropathies
- Urogenital Diseases
- Musculoskeletal Diseases
- Pathologic Processes
- Male Urogenital Diseases
- Kidney Diseases
- Urologic Diseases
- Female Urogenital Diseases
- Female Urogenital Diseases and Pregnancy Complications
- Arthritis
- Joint Diseases
- Genetic Diseases, Inborn
- Disease
- Renal Tubular Transport, Inborn Errors
- Syndrome
- Gitelman Syndrome
- Chondrocalcinosis
Other Study ID Numbers
- 2021-0670
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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