Key Insights

Highlights

Success Rate

93% trial completion (above average)

Published Results

25 trials with published results (16%)

Research Maturity

114 completed trials (73% of total)

Clinical Risk Assessment

Based on trial outcomes

Moderate Risk

Score: 50/100

Termination Rate

5.1%

8 terminated out of 157 trials

Success Rate

93.4%

+6.9% vs benchmark

Late-Stage Pipeline

10%

15 trials in Phase 3/4

Results Transparency

22%

25 of 114 completed with results

Key Signals

25 with results93% success

Data Visualizations

Phase Distribution

94Total
Not Applicable (68)
Early P 1 (1)
P 1 (3)
P 2 (7)
P 3 (4)
P 4 (11)

Trial Status

Completed114
Unknown23
Terminated8
Recruiting6
Active Not Recruiting4
Not Yet Recruiting1

Trial Success Rate

93.4%

Benchmark: 86.5%

Based on 114 completed trials

Clinical Trials (157)

Showing 20 of 20 trials
NCT05477719Not ApplicableCompletedPrimary

Effect of Compression Stockings on the Number of Apneas/Hypopneas Per Hour of Sleep in Patients With Syndrome Obstructive Sleep Apnea/Hypopnea as Compared to no Treatment

NCT04186078RecruitingPrimary

Clinical Characteristics of Patients With Sleep Apnea in Korea

NCT05382754Not ApplicableRecruiting

Home Apnea Testing in CHildren Trial

NCT04948541Not ApplicableCompleted

Effect Of Sleep Apnea Treatment On Temporo-Mandibular Disorders

NCT04007796Phase 2CompletedPrimary

Apnea and Insomnia Relief Study

NCT04234828Active Not RecruitingPrimary

Validation of Withings Sleep for the Detection of Sleep Apnea Syndrome

NCT03985527Not ApplicableCompletedPrimary

Janus Feasibility Study

NCT05516524Not ApplicableCompleted

HSAT for OSA Management in Children

NCT06578390Not ApplicableRecruitingPrimary

Efficacy Investigation of the Medical Device Apneal® on Smartphone for Sleep Apnea-Hypopnea Syndrome Diagnosis

NCT06474143Not ApplicableCompletedPrimary

Evaluation of the Clinical Performance of Apneal®, a Medical Device on Smartphone, for Sleep Apnea-hypopnea Syndrome Diagnosis.

NCT05056766CompletedPrimary

How Does the Clinical and Paraclinical Efficacy of an Oral Appliance Evolved According to Propulsion: Control With Each mm of Advancement

NCT05150470Not ApplicableCompletedPrimary

Evaluation of the Dental Movements Caused by Oral Appliance in Sleep Apnea Syndrome

NCT06535932Not ApplicableCompletedPrimary

Amara View Benchmark Study

NCT01005940Not ApplicableCompletedPrimary

Dental Device for Treatment of Sleep Apnea

NCT07086599Recruiting

Typological Study of Sleep Pathologies During Psoriatic Rheumatism and SAPHO Syndrome: Prospective Study Within the Paris Saint-Joseph Hospital Group"

NCT06141967Not ApplicableCompletedPrimary

Evaluating of the Impact of a Connected and Non-intrusive Device in Improving the Screening of Sleep Apnea Syndrome and the Addressing of Potentially Pathological Patients in Hospital Environment

NCT04688125Completed

Evaluation of An Optical Measurement Algorithm Combined With Patient and Provider Input to Reduce Mask Exchanges During Initial Positive Airway Pressure Therapy

NCT04399200Recruiting

Apnea, Stroke and Incident Cardiovascular Events

NCT06635265Not ApplicableCompleted

A Study to Determine the Flow Changes And/or AHI Reduction When Stimulating Two Targets (neural And/or Muscular) for the Treatment of Obstructive Sleep Apnea in Adult Subjects

NCT06627127Not ApplicableRecruiting

A Study to Investigate the Feasibility and Respiratory Effects of Stimulating Two Functional Targets (neural And/or Muscular) for the Treatment of Obstructive Sleep Apnea

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