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NCT04344899 · ClinicalTrials.gov registry record

Pediatric Oncology Recovery Trial After Surgery

A clinical trial of Pelvic Cancer, sponsored by University of Colorado, Denver.

Completed
Registry status
74
Enrollment target
3
Study locations

NCT04344899 is a study of Pelvic Cancer that has completed, run by University of Colorado, Denver. The registered enrollment target is 74 participants, above the 56-participant average among 6 other Pelvic Cancer trials with a reported enrollment target (32% higher). The trial reports 3 study locations across 3 states.

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The verdict

NCT04344899, a study of Pelvic Cancer, has completed, sponsored by University of Colorado, Denver.

COMPLETED
Registry status
74 participants
Enrollment target
3
Study locations

Study Summary

Pediatric Oncologic Recovery Trial After Surgery (PORTS) trial is an investigator-initiated, multicenter, multidisciplinary prospective case-control study of the implementation of an Enhanced Recovery After Surgery (ERAS) protocol at five tertiary-care pediatric hospitals in pediatric patients undergoing abdominal or retroperitoneal surgical resections for cancer. A pilot phase will determine characteristics of a successful protocol implementation and an exploratory phase plans to examine adherence, objective patient outcomes, and patient-reported outcomes. After completing primary enrollment, this collaborative will continue to enroll patients in the shared data registry and continue to refine the underlying ERAS protocol developed for this project.

Conditions Studied

Interventions

  • OTHER Observational

Study Locations (3)

Colorado

  • Children's Hospital Colorado - Aurora

Ohio

  • Cincinnati Children's Hospital Medical Center - Cincinnati

Tennessee

  • St Jude Children's Research Hospital - Memphis

Trial Details

FieldValue
Enrollment Target 74 participants
Start Date 2019-07-23
Est. Completion 2025-03-11

Sponsor

University of Colorado, Denver

1,283 total trials

What the Registry Record Tells You About NCT04344899

The ClinicalTrials.gov registry entry for NCT04344899 describes a study currently listed as completed, categorized as an unspecified phase. The registered enrollment target is 74 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 56-participant average among 6 other Pelvic Cancer trials with a reported enrollment target (32% higher). The listed sponsor is University of Colorado, Denver, which has 1,283 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Pelvic Cancer appearing as the primary indexed condition, and to 1 intervention - of which Observational is the first listed.

NCT04344899 reports 3 study locations spanning 3 distinct geographic areas - top geographies include Colorado, Ohio, Tennessee.

Frequently Asked Questions

What is clinical trial NCT04344899 about?

NCT04344899 is a clinical study titled "Pediatric Oncology Recovery Trial After Surgery". Pediatric Oncologic Recovery Trial After Surgery (PORTS) trial is an investigator-initiated, multicenter, multidisciplinary prospective case-control study of the implementation of an Enhanced Recovery After Surgery (ERAS) protocol at five tertiary-care pediatric hospitals in pediatric patients under...

What is the current status of trial NCT04344899?

This trial is currently completed. The enrollment target is 74 participants. The study started on 2019-07-23. Estimated completion is 2025-03-11.

What conditions does trial NCT04344899 study?

This clinical trial studies the following conditions: Pelvic Cancer.

What interventions are being tested in trial NCT04344899?

The interventions under investigation include: Observational (OTHER).

Who is sponsoring clinical trial NCT04344899?

This trial is sponsored by University of Colorado, Denver, which has 1,283 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT04344899 being conducted?

This trial has 3 study locations across Colorado, Ohio, Tennessee. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.