RECRUITING

Pediatric Oncology Recovery Trial After Surgery

Conditions

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

Pediatric Oncology Recovery Trial After Surgery

Quick Facts

Study Start:2019-07-23
Study Completion:2028-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT04344899

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:1 Month to 18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:CHILD, ADULT
Inclusion CriteriaExclusion Criteria
  1. * Patients undergoing operations at a pediatric hospital setting aged 1 month or older
  2. * Parents of patients undergoing operations at pediatric hospital settings aged 1 month or older
  3. * Undergoing urologic reconstruction, ureteral operations, pyeloplasty, intraabdominal on-cologic resections, urachal remnant excision, bariatric operations, pectus surgery, ap-pendicitis, orthopedic or neurosurgical operations and inflammatory bowel disease proce-dures
  4. * Providers of patients undergoing surgery in pediatric settings
  1. * Less than 1 month in age

Contacts and Locations

Study Contact

Jennifer Pyrzanowski
CONTACT
1.303.724.0769
jennifer.pyrzanowski@cuanschutz.edu

Principal Investigator

Kyle Rove, MD
PRINCIPAL_INVESTIGATOR
Childrens Hospital Colorado

Study Locations (Sites)

Children's Hospital Colorado
Aurora, Colorado, 80045
United States
Cincinnati Children's Hospital Medical Center
Cincinnati, Ohio, 45229
United States
St Jude Children's Research Hospital
Memphis, Tennessee, 38105
United States

Collaborators and Investigators

Sponsor: University of Colorado, Denver

  • Kyle Rove, MD, PRINCIPAL_INVESTIGATOR, Childrens Hospital Colorado

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2019-07-23
Study Completion Date2028-01

Study Record Updates

Study Start Date2019-07-23
Study Completion Date2028-01

Terms related to this study

Additional Relevant MeSH Terms

  • Pelvic Cancer