RECRUITING

Optimizing Pain Control in Transurethral Resection of the Prostate

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

The purpose of this study is to develop a multi-modal protocol for pain management after TURP that minimizes opioid use. The investigators hypothesize this approach will provide non-inferior pain control to the current standard of care which includes opioids as the primary agent. The investigators believe this is an important step in reducing the opioid epidemic in surgical patients.

Official Title

Optimizing Pain Control in Transurethral Resection of the Prostate

Quick Facts

Study Start:2017-12-08
Study Completion:2019-12-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT04102566

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:MALE
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Are identified as candidates for TURP
  2. * Are 18 years of age or greater
  3. * Are proficient in English
  1. * Have filled an opioid prescription in the last 2 months
  2. * Have an allergy to a medication included in the protocol
  3. * Have a history of pelvic radiation
  4. * Have renal failure (Serum Cr \> 2.0 mg/dl), peptic ulcer disease, history of gastric bypass, cirrhosis, or other contraindication precluding use of NSAID's
  5. * Have liver failure, hepatitis, or alcohol abuse which precludes use of acetaminophen

Contacts and Locations

Study Contact

Ryan Donahue, MD
CONTACT
2062236600
ryan.donahue@vmmc.org

Study Locations (Sites)

Virginia Mason Medical Center
Seattle, Washington, 98101
United States

Collaborators and Investigators

Sponsor: Benaroya Research Institute

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 Date2017-12-08
Study Completion Date2019-12-01

Study Record Updates

Study Start Date2017-12-08
Study Completion Date2019-12-01

Terms related to this study

Keywords Provided by Researchers

  • postoperative pain
  • Transurethral resection of the prostate
  • Multimodal pain control

Additional Relevant MeSH Terms

  • Pain
  • BPH With Urinary Obstruction
  • BPH With Urinary Obstruction With Other Lower Urinary Tract Symptoms