A Study to Collect Patient Data Collected Through Standard of Care Clinical Visits on the Subject of Hydronephrosis (Common Pediatric Urological Disorder that is Detected Prenatally, or Postnatal Infancy)


About this study

The purpose of this research study is to contribute to an existing registry that was developed by Virginia Commonwealth University (VCU). The registry will warehouse data points for patients detected prenatally or postnatally with hydronephrosis.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria:

  • Patients of age 18 to 65 will be asked to be in this study because they are pregnant and their fetus has hydronephrosis or if they have a child who has hydronephrosis.
  • Mothers under 18 will not be enrolled.
  • All children will be under the age of 6.

Exclusion Criteria:

  • Anyone who doesn’t carry the hydronephrosis condition.  
  • Who denies consent.

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status

Rochester, Minn.

Mayo Clinic principal investigator

Patricio Gargollo, M.D.

Closed-enrolling by invitation

What is this? (?)
Not open to everyone who meets the eligibility criteria, but only those invited to participate by the study team.

More information


Publications are currently not available

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