Actively Recruiting

Age: 18Years - 65Years
All Genders
NCT04625569

Genetic of Response to Acute Saline Load Test in Hypertension (Naload)

Led by Ospedale San Raffaele · Updated on 2024-05-14

150

Participants Needed

1

Research Sites

325 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

NHP referred to our outpatient clinic will be enrolled (150 newly recruited) in acute saline test for phenotype characterisation of PNat relationship(7). For each patient we will collect urine and blood samples for standard clinical biochemistry, including electrolytes, creatinine, EO, aldosterone, plasma renin activity, urinary uromodulin (ELISA), urinary and serum uric acid and blood samples for genetic test.

CONDITIONS

Official Title

Genetic of Response to Acute Saline Load Test in Hypertension (Naload)

Who Can Participate

Age: 18Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age between 18 and 65 years
  • Body mass index (BMI) less than 30 kg/m2
  • Sodium intake less than 300 mEq/24 hours based on urinary sodium excretion
  • Office systolic blood pressure over 140 mm Hg and diastolic blood pressure over 90 mm Hg measured in 3 consecutive visits to their family doctors
Not Eligible

You will not qualify if you...

  • Female patients
  • History of myocardial infarction
  • History of stroke
  • History of congestive heart failure
  • Liver disease
  • Secondary causes of hypertension
  • Diabetes
  • Severe hypertension with blood pressure over 160/110 mm Hg
  • Abuse of drugs or alcohol
  • Creatinine clearance less than 80 mL/min
  • Secondary forms of hypertension ruled out with specific investigations when appropriate

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 Ospedale San Raffaele

Milan, Italy, 20132

Actively Recruiting

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Research Team

C

Chiara Lanzani, doctor

CONTACT

C

Cinzia Scotti, secretary

CONTACT

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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