This study is currently not recruiting participants.

Long Term Success Rate of Laparoscopic and Robotic Dismembered Pyeloplasty for UPJ Obstruction

Investigating Kidney Longevity After Surgery for Ureteropelvic Junction Obstruction

Not Recruiting
100 years or below
All
Phase N/A
1 Location

Brief description of study.

The purpose of this study is to observe the longevity and durability of a kidney over a five to ten-year period after it has undergone laparoscopic or robotic dismembered pyeloplasty for ureteropelvic junction obstruction.

Detailed description of study

The purpose of this study is to observe the longevity and durability of a kidney over a five to ten-year period after it has undergone laparoscopic or robotic dismembered pyeloplasty for ureteropelvic junction obstruction.

Eligibility of study

You may be eligible for this study if you meet the following criteria:

  • Conditions: UPJ Obstruction
  • Age: 100 years or below
  • Gender: All

This study investigates the long-term health of kidneys after surgery for ureteropelvic junction obstruction, a condition where the connection between the kidney and the ureter is blocked. The study focuses on two surgical methods: laparoscopic and robotic dismembered pyeloplasty, which are minimally invasive procedures used to correct this blockage.

Participants will undergo regular assessments to monitor kidney function over a period of five to ten years. These assessments will help determine how well the kidney functions after surgery and the durability of the surgical repair over time.

  • Who can participate: Participants must meet specific eligibility criteria, including age requirements. Key factors include a diagnosis of ureteropelvic junction obstruction requiring surgical intervention.
  • Study details: Participants will be monitored to evaluate kidney function following surgery. The study focuses on the outcomes of laparoscopic or robotic dismembered pyeloplasty.
  • Study Timelines: The study will last five to ten years.
Updated on 19 Feb 2024. Study ID: 1408920892

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