Actively Recruiting

Age: 18Years +
All Genders
NCT06869603

Evaluation of Adherence to the Mediterranean Diet in Patients with Recurrent Renal Stones and Disease Osteometabolic

Led by IRCCS SYNLAB SDN · Updated on 2025-03-11

50

Participants Needed

1

Research Sites

155 weeks

Total Duration

On this page

Sponsors

I

IRCCS SYNLAB SDN

Lead Sponsor

D

Department of Clinical Medicine and Surgery - University of Naples Federico II

Collaborating Sponsor

AI-Summary

What this Trial Is About

The aim of this research protocol is to evaluate the adherence to the Mediterranean diet in patients suffering from recurrent kidney stones and osteometabolic diseases. Results of the study will allow to assess the dietary habits of patients with the above diseases. Given the universal prevalence of nephrolithiasis and osteometabolic diseases, the knowledge of these data appears crucial for the proper management of the dietary approach to prophylaxis secondar

CONDITIONS

Official Title

Evaluation of Adherence to the Mediterranean Diet in Patients with Recurrent Renal Stones and Disease Osteometabolic

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients with idiopathic relapsing nephrolithiasis with bilateral renal stones confirmed by imaging or who have passed more than one stone in the past 5 years
Not Eligible

You will not qualify if you...

  • Patients with albumin-corrected plasma calcium levels greater than 11.0 mg/dl at the time of first vitamin D measurement
  • Patients with glomerular filtration rate less than 60 mL/min/1.73 m2
  • Patients with a personal history of chronic granulomatous disease
  • Pregnant patients
  • Patients with known morphological abnormalities of the excretory system
  • Patients with incomplete data collection

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Irccs Synlab Sdn

Naples, Italy, 80143

Actively Recruiting

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How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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