Actively Recruiting

Age: 18Years +
All Genders
NCT01873235

PKD Clinical and Translational Core Study

Led by University of Maryland, Baltimore · Updated on 2025-09-11

350

Participants Needed

1

Research Sites

900 weeks

Total Duration

On this page

Sponsors

U

University of Maryland, Baltimore

Lead Sponsor

N

National Institutes of Health (NIH)

Collaborating Sponsor

AI-Summary

What this Trial Is About

Advances in our understanding of the pathogenesis of autosomal dominant polycystic kidney disease (ADPKD) have opened up possibilities of new therapies to prevent disease progression. High quality clinical investigations in patients with ADPKD, however, pose significant challenges to investigators including limited access to patients with ADPKD,insufficient guidance by experienced investigators and lack of resources to conduct these studies. The Polycystic Kidney Disease Research Clinical and Translational Core (P30) aims to establish an infrastructure that will assist investigators in designing and conducting highest quality clinical and translational research focused on a diverse group of patients with ADPKD. Objective 1: To establish a Mid-Atlantic cohort of ADPKD patients (N=350) with baseline clinical phenotyping performed at the General Clinical Research Unit of the University of Maryland School of Medicine. Objective 2: To establish a state-of-the-art biobank of specimens from the ADPKD cohort including serum, plasma,urine and DNA. Objective 3: To develop a collaborative network of physicians and practices in the Mid-Atlantic region who will contribute to the ADPKD cohort and will be willing to refer patients for future studies and trials. Objective 4: To establish a web-based registry of ADPKD patients in the Mid-Atlantic area.

CONDITIONS

Official Title

PKD Clinical and Translational Core Study

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 and older
  • ADPKD confirmed by genetic testing or ultrasound using modified Ravine criteria
  • Ability to provide written informed consent and comply with study requirements
  • Glomerular Filtration Rate (GFR) greater than 15 ml/min/1.73m2
Not Eligible

You will not qualify if you...

  • End Stage Renal Disease, currently on dialysis, or prior kidney transplant
  • Pregnant, lactating, or planning pregnancy within 6 weeks
  • Presence of another systemic disease such as cancer or lupus
  • Life expectancy less than 2 years
  • Participation in a drug treatment trial
  • Non-English speaking
  • Uncontrolled diabetes (A1C 7.0 or higher within 6 months or on more than one oral hypoglycemic agent)
  • Diabetic nephropathy

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

University of Maryland School of Medicine General Clinical Research Center

Baltimore, Maryland, United States, 21201

Actively Recruiting

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Research Team

C

Charalett E Diggs, RN, MSN

CONTACT

K

Karkleen Schuhart

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

1

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