Sinopsys Lacrimal Stent Indicated for Sinus Irrigation
NCT02297243 · Status: COMPLETED · Phase: EARLY_PHASE1 · Type: INTERVENTIONAL · Enrollment: 9
Last updated 2016-02-12
Summary
The purpose of this study is to collect preliminary clinical data related to the safety and performance of the Sinopsys Lacrimal Stent.
Conditions
- Ethmoid Sinusitis
Interventions
- DEVICE
-
Sinopsys Lacrimal Stent
The Sinopsys Lacrimal Stent is indicated for use to create a transcaruncular ethmoid sinus access.
Sponsors & Collaborators
-
Sinopsys Surgical
lead INDUSTRY
Principal Investigators
-
Teena Augustino · Sinopsys Surgical Inc.
Study Design
- Allocation
- NA
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 22 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2015-03-31
- Primary Completion
- 2016-02-29
- Completion
- 2016-02-29
Countries
- United States
Study Locations
More Related Trials
-
Clinical Evaluation of the Steroid-Eluting Sinexus Intranasal Splint When Used Following Functional Endoscopic Sinus Surgery (FESS) in Patients With Chronic Sinusitis
NCT00912405 ·Status: COMPLETED ·Phase: NA
-
Safety and Performance of the SinuSys Dilation System for Dilation of the Maxillary Sinus Ostium
NCT01623050 ·Status: COMPLETED ·Phase: PHASE1
-
Safety and Efficacy of the Propel Mini and Propel Nova Steroid-Eluting Sinus Implant in Frontal Sinus
NCT02266810 ·Status: COMPLETED ·Phase: PHASE3
-
Comparison of Two Steroid Nasal Implants Following Endoscopic Sinus Surgery for Chronic Rhinosinusitis
NCT03729310 ·Status: WITHDRAWN ·Phase: EARLY_PHASE1
-
Study Designed to Clinically Evaluate Sinus Wash Device Prototypes
NCT02931604 ·Status: UNKNOWN ·Phase: NA
-
A Clinical Evaluation of the Sinexus Intranasal Splint Following Functional Endoscopic Sinus Surgery in Patients With Chronic Rhinosinusitis
NCT00840970 ·Status: COMPLETED ·Phase: NA
-
Gel-Sinuplasty for Chronic Rhinosinusitis With and Without Nasal Polyposis
NCT03472144 ·Status: UNKNOWN ·Phase: PHASE3
-
Results of Endoscopic Sinus Surgery in Management of Ophthalmological Complications of Chronic Rhino Sinusitis
NCT04617223 ·Status: COMPLETED ·Phase: NA
-
Efficacy of Post-FESS Implantation of Composite Removable Sinus Stent to Prevent Post-Operative Complications
NCT02812199 ·Status: UNKNOWN ·Phase: NA
-
Sinonasal Therapies and Histologic Correlations of Patients With Cystic Fibrosis in the Era of Highly Effective Modulator Therapy
NCT06996951 ·Status: RECRUITING ·Phase: PHASE3
-
Safety and Effectiveness Evaluation of the Sinusway Device for Endoscopy of the Nasal Cavity and Paranasal Sinuses
NCT02502084 ·Status: COMPLETED ·Phase: NA
-
Treatment Decision-Making Among Patients With Chronic Rhinosinusitis
NCT07010679 ·Status: ENROLLING_BY_INVITATION ·Phase: NA
-
Treatment of Nasal Airway Obstruction Using the Aerin Medical Device
NCT02914236 ·Status: COMPLETED ·Phase: NA
-
Clinical Study of Safety and Efficacy for the Relieva Stratus With Elution of Triamcinolone Acetonide
NCT00791934 ·Status: COMPLETED ·Phase: NA
-
Clinical Evaluation of Propel Nova Sinus Implant in Peripheral Sinus Ostia
NCT02228720 ·Status: COMPLETED ·Phase: NA
-
ENTact™ Septal Stapler Shelf Life Extension
NCT00957502 ·Status: COMPLETED ·Phase: NA
-
Safety and Efficacy of Balloon Sinuplasty in Pediatric Sinusitis
NCT00939471 ·Status: COMPLETED ·Phase: NA
-
Sinus Balloon Dilation in Pediatric Patients
NCT02278484 ·Status: COMPLETED ·Phase: NA
-
Gold Laser Vs. Micro-Debriders for Functional Endoscopic Sinus Surgery
NCT02900794 ·Status: WITHDRAWN ·Phase: NA
-
A User Study of SYNUS Pain Relief Made by Tivic Health Systems
NCT03466879 ·Status: COMPLETED
-
Spirox Latera™ Implant Support of Lateral Nasal Wall Cartilage (LATERAL-OR) Study
NCT02952313 ·Status: COMPLETED ·Phase: NA
-
Steroid Delivery to the Frontal Sinus Opening With a Bioabsorbable Implant vs. a Bioabsorbable Nasal Dressing
NCT03188822 ·Status: TERMINATED ·Phase: NA
-
Anti-Inflammatory Agent in Sinusitis
NCT02874144 ·Status: COMPLETED ·Phase: PHASE2
-
Steroid-eluting Sinus Stent for Chronic Rhinosinusitis Patients With Uncontrolled Postoperative Symptoms
NCT06198894 ·Status: RECRUITING ·Phase: NA
-
Study of the ENTact Septal Staple System for Tissue Approximation During Septoplasty
NCT00740480 ·Status: COMPLETED