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Clinical trialNCT02964312CompletedInterventional

LATERA-OFFICE Study

SponsorSpirox, Inc.Enrollment166Nasal Obstruction
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

Prospective, multicenter, nonrandomized, single-arm controlled study to obtain outcomes data in participants with severe to extreme class NOSE scores who are undergoing placement of the Spirox Latera Implant with or without concurrent turbinate reduction procedures in an office setting.

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

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

United States
  • Alessi Institute for Facial Plastic Surgery

    Beverly Hills, California, United States

  • Beverly Hills Aesthetic Surgical Institute

    Beverly Hills, California, United States

  • Ent Assoc. of South Florida

    Boca Raton, Florida, United States

  • the Center for Sinus, Allergy, & Sleep Wellness

    Boynton Beach, Florida, United States

  • Ent of Georgia

    Atlanta, Georgia, United States

  • Chicago Nasal & Sinus Center

    Chicago, Illinois, United States

  • Madison Ent & Facial Plastic Surgery

    New York, New York, United States

  • Collin County Ent

    Frisco, Texas, United States

  • Ogden Clinic

    Ogden, Utah, 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
10 Nov 2016
Primary completion
21 Mar 2018
Completion
29 Aug 2019
Last update posted
3 Sept 2020
Registered enrollment
166
Registry id
NCT02964312

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.