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Clinical trialNCT01253577CompletedPhase 3Interventional

A Clinical Evaluation of a Steroid-Coated Sinus Stent When Used Following Functional Endoscopic Sinus Surgery in Patients With Chronic Sinusitis

SponsorIntersect ENTEnrollment105Chronic Sinusitis
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

The purpose of this study is to assess the safety and efficacy of the Propel mometasone furoate implant when used following Functional Endoscopic Sinus Surgery (FESS) in patients with Chronic Sinusitis (CS).
clinicaltrials.gov ↗

Investigators

The overall officials registered on this study. Names that resolve to a findmyKOL profile link to it; the rest are shown as registered.

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

11 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

United States
  • Central California Ent

    Fresno, California, United States

  • Colorado Ent & Allergy

    Colorado Springs, Colorado, United States

  • Northwestern University

    Chicago, Illinois, United States

  • Northshore University Health System

    Evanston, Illinois, United States

  • Advanced Ent & Allergy

    Louisville, Kentucky, United States

  • Charlotte Eye, Ent Associates

    Charlotte, North Carolina, United States

  • Austin Ent Clinics

    Austin, Texas, United States

  • University of Texas Sw Medical School

    Dallas, Texas, United States

  • University of Texas Medical School

    Houston, Texas, United States

  • Intermountain Ent

    Salt Lake City, Utah, United States

  • Eastern Virgina Medical School

    Norfolk, Virginia, United States

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

No drug or biological interventions are in our data for this study. It may test a procedure, device or behavioral intervention, or the intervention list isn't in our current snapshot. See the registry record ↗. Why? →

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
31 Dec 2009
Primary completion
31 Oct 2010
Completion
31 Oct 2010
Last update posted
22 Jun 2015
Registered enrollment
105
Registry id
NCT01253577
clinicaltrials.gov ↗

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 24 Aug 2026. Registry facts are shown as registered by the study sponsor; findmyKOL does not interpret them.