Key Insights

Highlights

Success Rate

100% trial completion (above average)

Clinical Risk Assessment

Based on trial outcomes

Moderate Risk

Score: 40/100

Termination Rate

0.0%

0 terminated out of 26 trials

Success Rate

100.0%

+13.4% vs benchmark

Late-Stage Pipeline

12%

3 trials in Phase 3/4

Results Transparency

0%

0 of 3 completed with results

Key Signals

100% success

Data Visualizations

Phase Distribution

19Total
Not Applicable (13)
P 1 (2)
P 2 (1)
P 3 (3)

Trial Status

Recruiting10
Not Yet Recruiting8
Enrolling By Invitation3
Completed3
Withdrawn2

Trial Success Rate

100.0%

Benchmark: 86.6%

Based on 3 completed trials

Clinical Trials (26)

Showing 20 of 20 trials
NCT07119879CompletedPrimary

Impact of Climate Change Anxiety on Sinusitis Symptoms and Quality of Life Among Adults With Chronic Rhinosinusitis: A Cross-Sectional Study

NCT07714525Phase 2RecruitingPrimary

Triamcinolone Nanocapsules After Endoscopic Nasal Surgery

NCT07681973Not ApplicableRecruiting

Cognitive and Immunologic Profiles of Patients With Olfactory Dysfunction After Smell Training

NCT07286201Not ApplicableEnrolling By InvitationPrimary

Evaluation of the Safety and Performance of a Bioresorbable Nasal Dressing Containing Mometasone Furoate (MF)

NCT07645521Not ApplicableCompletedPrimary

Trans-nasal Sphenopalatine Ganglion Block for Prevention of Emergence Agitation Following Functional Endoscopic Sinus Surgery

NCT07599826Not ApplicableNot Yet Recruiting

Active vs. Passive VR During Office-based ENT Procedures

NCT07546682RecruitingPrimary

Propel Drug-Eluting Sinus Implant Family IBUKI Cohort

NCT07460934Not ApplicableCompletedPrimary

Effect of Pleuran on the Clinical Course of Patients With Chronic Rhinosinusitis

NCT07386873Not ApplicableNot Yet RecruitingPrimary

The Efficacy of Olfactory Cleft Steroid Drops in Patients With CRS With Olfactory Cleft Obstruction

NCT07383402Phase 3Not Yet RecruitingPrimary

Intra-Sinus Povidone-Iodine and Budesonide After Endoscopic Sinus Surgery for Chronic Rhinosinusitis

NCT07299474Not ApplicableRecruiting

Efficacy of Lavender Aromatherapy on Anxiety and Pain Reduction During Awake Otolaryngologic Procedures

NCT07010679Not ApplicableEnrolling By InvitationPrimary

Treatment Decision-Making Among Patients With Chronic Rhinosinusitis

NCT06996951Phase 3Recruiting

Sinonasal Therapies and Histologic Correlations of Patients With Cystic Fibrosis in the Era of Highly Effective Modulator Therapy

NCT07262450Not ApplicableRecruiting

Assessement of Effectiveness of Seawater Nasal Sprays on Sinonasal Symptoms

NCT07259538Phase 1RecruitingPrimary

A Phase I Study Evaluating the Safety, Tolerability, and Pharmacokinetics of VVN432 Nasal Spray

NCT07049978Not Yet Recruiting

Long-term Effect of Dupilumab in N-ERD

NCT06815211Not Yet RecruitingPrimary

The German National CRS Registry (GenreCRS): Clinical Evaluation of the New European Academy for Allergy and Clinical Immunology (EAACI) Criteria for CRSwNP Disease Control, Remission and Cure in a Real-World Evidence Study Approach

NCT06750302Phase 1RecruitingPrimary

Effectiveness of Penthrox vs Placebo in Sinus Procedures, a Clinical Trial

NCT06671561WithdrawnPrimary

Product Surveillance Registry; Ear, Nose and Throat - EXTEND Cohort

NCT06960876Not ApplicableRecruitingPrimary

Comparative Effects of Therapeutic Ultrasound and Sinus Massage in Chronic Rhinosinusitis: a Randomized Controlled Study

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