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RECRUITING Phase 4

Optimizing Pain Control in Transurethral Resection of the Prostate

NCT04102566 · View on ClinicalTrials.gov ↗

Study Summary

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.

Interventions

  • DRUG Ibuprofen 600 mg
  • BEHAVIORAL Education

Study Locations (1)

Washington

  • Virginia Mason Medical Center — Seattle

Trial Details

FieldValue
Enrollment Target 50 participants
Start Date 2017-12-08
Est. Completion 2019-12-01
Phase Phase 4

Sponsor

Benaroya Research Institute

12 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT04102566

The ClinicalTrials.gov registry entry for NCT04102566 describes a study currently listed as recruiting. It is categorized as Phase 4, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 50 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Benaroya Research Institute, which has 12 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 3 conditions, with Pain appearing as the primary indexed condition, and to 2 interventions — of which Ibuprofen 600 mg is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT04102566 reports 1 study location spanning 1 distinct geographic area — top geographies include Washington. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT04102566 about?

NCT04102566 is a clinical study titled "Optimizing Pain Control in Transurethral Resection of the Prostate". 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 b...

What is the current status of trial NCT04102566?

This trial is currently recruiting. It is a Phase 4 study. The enrollment target is 50 participants. The study started on 2017-12-08. Estimated completion is 2019-12-01.

What conditions does trial NCT04102566 study?

This clinical trial studies the following conditions: Pain, BPH With Urinary Obstruction, BPH With Urinary Obstruction With Other Lower Urinary Tract Symptoms. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT04102566?

The interventions under investigation include: Ibuprofen 600 mg (DRUG), Education (BEHAVIORAL). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT04102566?

This trial is sponsored by Benaroya Research Institute, which has 12 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT04102566 being conducted?

This trial has 1 study location across Washington. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

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