Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

ACTIVE NOT RECRUITING

Pediatric Urology Recovery After Surgery Endeavor (PURSUE)

NCT03245242 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this research study is to evaluate an Enhanced Recovery After Surgery (ERAS) protocol in children and young adults undergoing urologic reconstructive surgery. The investigators plan to collect data on speed of recovery (how quickly pain improves, length of time in the hospital, and the need for additional pain control) on patients who receive care under the ERAS protocol and compare it to historical controls.

Interventions

  • OTHER Enhanced Recovery after Surgery
  • OTHER Historical usual surgical care

Study Locations (7)

Colorado

  • Children's Hospital Colorado — Aurora

Illinois

  • Ann & Robert Lurie Children's Hospital of Chicago — Chicago

Missouri

  • Washington University School of Medicine — St Louis

Ohio

  • Cincinnati Children's Hospital Medical Center — Cincinnati

Oklahoma

  • Oklahoma University Health Science Center — Oklahoma City

Pennsylvania

  • Children's Hospital of Pittsburgh of UPMC — Pittsburgh

Virginia

  • Children's Hospital of Richmond at Virginia Commonwealth University — Richmond

Trial Details

FieldValue
Enrollment Target 85 participants
Start Date 2017-04-01
Est. Completion 2026-10-31

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT03245242

The ClinicalTrials.gov registry entry for NCT03245242 describes a study currently listed as active not recruiting. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 85 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Washington University School of Medicine, which has 1,036 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 3 conditions, with Urinary Bladder, Neurogenic appearing as the primary indexed condition, and to 2 interventions — of which Enhanced Recovery after Surgery is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT03245242 reports 7 study locations spanning 7 distinct geographic areas — top geographies include Colorado, Illinois, Missouri. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT03245242 about?

NCT03245242 is a clinical study titled "Pediatric Urology Recovery After Surgery Endeavor (PURSUE)". The purpose of this research study is to evaluate an Enhanced Recovery After Surgery (ERAS) protocol in children and young adults undergoing urologic reconstructive surgery. The investigators plan to collect data on speed of recovery (how quickly pain improves, length of time in the hospital, and th...

What is the current status of trial NCT03245242?

This trial is currently active not recruiting. The enrollment target is 85 participants. The study started on 2017-04-01. Estimated completion is 2026-10-31.

What conditions does trial NCT03245242 study?

This clinical trial studies the following conditions: Urinary Bladder, Neurogenic, Urinary Bladder Diseases, Urologic Surgical Procedures. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT03245242?

The interventions under investigation include: Enhanced Recovery after Surgery (OTHER), Historical usual surgical care (OTHER). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT03245242?

This trial is sponsored by Washington University School of Medicine, which has 1,036 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT03245242 being conducted?

This trial has 7 study locations across Colorado, Illinois, Missouri, Ohio, Oklahoma. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial