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Recruiting NCT07511283

NCT07511283 Calciphylaxis in Patients With Chronic Kidney Disease - A Study of the Danish Calciphylaxis Research Initiative (DanCaRI)

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Clinical Trial Summary
NCT ID NCT07511283
Status Recruiting
Phase
Sponsor Odense University Hospital
Condition Calciphylaxis
Study Type OBSERVATIONAL
Enrollment 860 participants
Start Date 2026-04
Primary Completion 2040-06

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type OBSERVATIONAL

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 860 participants in total. It began in 2026-04 with a primary completion date of 2040-06.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

Calciphylaxis is a rare yet life-threatening condition involving pronounced calcification in small blood vessels of the skin. Knowledge about its underlying mechanisms and contributing risk factors remains limited. Chronic kidney disease is one of the strongest disease predictors. No evidence based effective therapy is currently available. Research on the topic is mainly hindered by the condition's rarity. The study Calciphylaxis in patients with chronic kidney disease - A study of the Danish Calciphylaxis Research Initiative (DanCaRI) is set up to facilitate the systematic retrospective and prospective comparison of patients with chronic kidney disease and calciphylaxis to matched patients with chronic kidney disease who did not develop calciphylaxis thereby providing new knowledge that can support prevention, early detection, and new treatment approaches.

Eligibility Criteria

Inclusion Criteria: Cases * Age ≥18 years. * CKD. * Suspicion of calciphylaxis or newly diagnosed calciphylaxis episode. The suspicion or diagnosis of calciphylaxis is a mutual decision of the involved medical specialties (nephrologist, dermatologist, pathologist, other). * Ability to give informed consent. * Ability to participate in a clinical study as assessed by the local investigator. * Provides written informed consent. Controls * Age ≥18 years. * CKD * Ability to give informed consent. * Ability to participate in a clinical study as assessed by the local investigator. * Provides written informed consent. Healthy reference group * Age ≥18 years. * Self-assessed as healthy, confirmed by local investigators at inclusion Exclusion Criteria: Cases \- the calciphylaxis diagnosis becomes excluded Controls - Being diagnosed with calciphylaxis Healthy controls Up to 60 years of age: eGFR below 60 ml/min/1.72m2. \- Over 60 years of age: eGFR below the 95% confidence interval for eGFR adjusted for age (Danish Society of Nephrology references ranges)

Contact & Investigator

Central Contact

Subagini Nagarajah, PhD

✉ subagini.nagarajah3@rsyd.dk

📞 +45 40498337

Principal Investigator

Subagini Nagarajah, PhD

PRINCIPAL INVESTIGATOR

Odense University Hospital

Frequently Asked Questions

Who can join the NCT07511283 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Calciphylaxis. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07511283 currently recruiting?

Yes, NCT07511283 is actively recruiting participants. Contact the research team at subagini.nagarajah3@rsyd.dk for enrollment information.

Where is the NCT07511283 trial being conducted?

This trial is being conducted at Odense, Denmark.

Who is sponsoring the NCT07511283 clinical trial?

NCT07511283 is sponsored by Odense University Hospital. The principal investigator is Subagini Nagarajah, PhD at Odense University Hospital. The trial plans to enroll 860 participants.

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