RECRUITING

NXT Post-Market Clinical Follow-up

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

NXT Urodynamics System Post-Market Clinical Follow-up Clinical Investigation to Confirm Ongoing Safety and Performance in Urodynamic Patient Sub-Populations

Official Title

NXT Urodynamics System Post-Market Clinical Follow-up Clinical Investigation

Quick Facts

Study Start:2024-06-18
Study Completion:2025-12
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06336304

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:Not specified
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:CHILD, ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Patients medically indicated for urodynamic study
  2. * Patient or legally authorized representative provides written authorization and/or consent per institution and geographical requirements
  1. * Patients or legally authorized representative with cognitive or psychiatric condition that interferes with or precludes direct and accurate communication regarding the study, giving informed consent or ability to complete the patient questionnaire
  2. * Patients with confirmed active bladder infections (not including patients with asymptotic bacteria)
  3. * Pregnant women
  4. * Patients with recent (less than 2 weeks) pelvic floor surgery
  5. * Requires use of suprapubic catheter

Contacts and Locations

Study Contact

Kaitlyn Palm
CONTACT
6128160068
rs.nxtpmcf@laborie.com
Adele Campbell
CONTACT
6032558251
rs.nxtpmcf@laborie.com

Study Locations (Sites)

Chesapeake Urology Hanover
Hanover, Maryland, 21076
United States
Chesapeake Urology Owing Mills
Owings Mills, Maryland, 21117
United States

Collaborators and Investigators

Sponsor: Laborie Medical Technologies Inc.

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 Date2024-06-18
Study Completion Date2025-12

Study Record Updates

Study Start Date2024-06-18
Study Completion Date2025-12

Terms related to this study

Additional Relevant MeSH Terms

  • Urinary Incontinence
  • Urinary Obstruction
  • Urinary Bladder, Overactive
  • Urinary Bladder, Neurogenic
  • Urinary Incontinence, Urge