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Completed Phase 1 Interventional Results available

Safety and Performance of the SinuSys Dilation System for Dilation of the Maxillary Sinus Ostium

ClinicalTrials.gov ID: NCT01623050

Public ClinicalTrials.gov record NCT01623050. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 23, 2026, 5:26 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

SinuSys Patency of Maxillary Sinus Ostia Study

Study identification

NCT ID
NCT01623050
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Lead sponsor
SinuSys Corporation
Industry
Enrollment
36 participants

Conditions and interventions

Conditions

Interventions

  • SinuSys Dilation System Device

Device

Eligibility (public fields only)

Age range
18 Years to 75 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Mar 31, 2012
Primary completion
May 31, 2013
Completion
Aug 31, 2014
Last update posted
Nov 4, 2014

2012 – 2014

United States locations

U.S. sites
3
U.S. states
3
U.S. cities
3
Facility City State ZIP Site status
Valley ENT Tucson Arizona 85745
Palo Alto Medical Foundation Palo Alto California 94301
St. Elizabeth Medical Center Boston Massachusetts 02135

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 2 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01623050, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Nov 4, 2014 · Synced Jul 23, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01623050 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →