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COMPLETED Phase 2

Study of Silodosin to Facilitate Passage of Urinary Stones

NCT01144949 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this study is to assess if patients treated with silodosin will have a higher spontaneous passage rate of their ureteral stone than those treated with placebo.

Interventions

  • DRUG placebo
  • DRUG silodosin

Study Locations (20)

New York

  • Watson Investigational Site — Albany
  • Watson Investigational Site — Garden City
  • Watson Investigational Site — New York
  • Watson Investigational Site — Plainview
  • Watson Investigational Site — Syracuse

New Jersey

  • Watson Investigational Site — Hackensack
  • Watson Investigational Site — Mount Laurel
  • Watson Investigational Site — Sewell
  • Watson Investigational Site — Voorhees Township

California

  • Watson Investigative Site — Mission Hills
  • Watson Investigational Site — Murrieta
  • Watson Investigational Site — San Diego

Florida

  • Watson Investigational Site — Daytona Beach
  • Watson Investigational Site — Gainesville
  • Watson Investigational Site — Orange City

Alabama

  • Watson Investigational Site — Birmingham

Alaska

  • Watson Investigational Site — Anchorage

Kansas

  • Watson Investigative Site — Overland Park

Missouri

  • Watson Investigative Site — North Kansas City

Trial Details

FieldValue
Enrollment Target 239 participants
Start Date 2010-06
Est. Completion 2012-07
Phase Phase 2

Sponsor

Watson Pharmaceuticals

11 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT01144949

The ClinicalTrials.gov registry entry for NCT01144949 describes a study currently listed as completed. It is categorized as Phase 2, 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 239 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Watson Pharmaceuticals, which has 11 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 Kidney Stones appearing as the primary indexed condition, and to 2 interventions — of which placebo 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: NCT01144949 reports 20 study locations spanning 9 distinct geographic areas — top geographies include New York, New Jersey, California. 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 NCT01144949 about?

NCT01144949 is a clinical study titled "Study of Silodosin to Facilitate Passage of Urinary Stones". The purpose of this study is to assess if patients treated with silodosin will have a higher spontaneous passage rate of their ureteral stone than those treated with placebo.

What is the current status of trial NCT01144949?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 239 participants. The study started on 2010-06. Estimated completion is 2012-07.

What conditions does trial NCT01144949 study?

This clinical trial studies the following conditions: Kidney Stones, Urolithiasis, Ureteral Calculi. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT01144949?

The interventions under investigation include: placebo (DRUG), silodosin (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT01144949?

This trial is sponsored by Watson Pharmaceuticals, which has 11 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT01144949 being conducted?

This trial has 20 study locations across Alabama, Alaska, California, Florida, Kansas. 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