RECRUITING

HoLEP Prior to Radiation Therapy for Patients With LUTS/Retention and Concurrent Prostate Cancer

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

To determine if holmium laser enucleation of the prostate (HoLEP) for the treatment of lower urinary tract symptoms (LUTS) and/or urinary retention alters the treatment course for patients concurrently diagnosed with prostate cancer.

Official Title

HoLEP Prior to Radiation Therapy for Patients With LUTS/Retention and Concurrent Prostate Cancer

Quick Facts

Study Start:2019-09-19
Study Completion:2035-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT03802851

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:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Patients must be 18 years of age or older
  2. * Patients must have bothersome lower urinary tract symptoms (LUTS), defined by American Urological Association Symptom Score (AUA SS) of greater than or equal to 15 and/or as defined by a post-void residual of greater than or equal to 350mL and/or as defined by catheter dependence
  3. * Patients must be diagnosed with prostate cancer by pathological tissue analysis
  4. * Patients must have elected for radiation with androgen deprivation therapy as the primary treatment modality for their prostate cancer
  1. * Patients who are under 18 years of age are not eligible
  2. * Patients who have a diagnosis of bladder cancer are not eligible.
  3. * Patients with prior treatment for prostate cancer are not eligible.
  4. * Patients with any type of prior prostate surgery (minimally invasive, endoscopic, or otherwise) including prior transurethral resection of the prostate (but excluding prior prostate biopsy) are ineligible.
  5. * Patients with known metastatic prostate cancer are ineligible
  6. * Patients who are enrolled in other surgical or international trials at the time of this study are not eligible

Contacts and Locations

Study Contact

Jane Ledesma, BS
CONTACT
(913) 588-8721
jledesma2@kumc.edu

Principal Investigator

Bristol Whiles, MD
PRINCIPAL_INVESTIGATOR
University of Kansas Medical Center

Study Locations (Sites)

University of Kansas Health System
Kansas City, Kansas, 66160
United States

Collaborators and Investigators

Sponsor: University of Kansas Medical Center

  • Bristol Whiles, MD, PRINCIPAL_INVESTIGATOR, University of Kansas Medical Center

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 Date2019-09-19
Study Completion Date2035-01

Study Record Updates

Study Start Date2019-09-19
Study Completion Date2035-01

Terms related to this study

Additional Relevant MeSH Terms

  • Prostate Cancer
  • Lower Urinary Tract Symptoms