ResMed

25 total trials 1 currently recruiting 20 completed

ResMed sponsors 25 registered US clinical trials on ClinicalTrials.gov, 1 of them currently recruiting, and 20 completed. 1 of these trials are in Phase 3-4 (later-stage) and 0 in Phase 1-2 (earlier-stage). The most-studied condition in this pipeline is Obstructive Sleep Apnea, with 2 trials.

Trial Pipeline

25 total, page 1 of 1

RECRUITING NA

ASV Therapy for Insomnia

NCT07011966

COMPLETED NA

Oran Park Mask External Clinical Study (3) Marketing Claims Study

NCT06079866

COMPLETED NA

Whitsundays (Nasal) Mask Take Home Study (90 Days)

NCT06036329

COMPLETED NA

A Preference Study of Two Pneumatic Compression Devices for Patients With Lower Limb Lymphedema

NCT05485454

COMPLETED NA

Safety and Feasibility of a Novel Device for Assessing Respiratory Function in Children

NCT04873193

COMPLETED NA

Nebula Study - Screener Apps and HSAT vs. PSG Comparison

NCT04597749

COMPLETED NA

Evaluating the Efficacy of PAP Therapy for Treating OSA in the Home Environment

NCT04744038

COMPLETED NA

Compact Pneumatic Compression Device for Patients With Lymphedema

NCT04226287

COMPLETED NA

Evaluation of a Portable Oxygen Concentrator During Ambulation for Patients Who Require Supplemental Oxygen (POC-LEAN)

NCT04107493

COMPLETED NA

Evaluation of an Incentive-based Intervention to Improve 90-day Adherence in PAP-Naive Patients

NCT03851094

COMPLETED

Validation of ApneaLink Air Home Sleep Testing in the Diagnosis of Obstructive Sleep Apnea in Adolescent Children

NCT03748771

TERMINATED NA

Portable Oxygen Concentrator Improvements to Physical Activity, Oxygen Usage, and Quality of Life in Chronic Obstructive Pulmonary Disease Patients Using Long-term Oxygen Therapy (POC-STEP)

NCT03513068

COMPLETED NA

ApneaLink Air Home Sleep Testing (HST) Device Validation Study

NCT03470493

TERMINATED NA

Adherence to ASV Therapy in Heart Failure With Preserved Ejection Fraction Feasibility Study

NCT03195660

COMPLETED NA

Respiration Rate Monitoring in COPD Patients

NCT03030313

COMPLETED Phase 3

Astral VAPS AutoEPAP Clinical Trial

NCT02683772

TERMINATED NA

Reassure Remote Respiration Monitoring in Heart Failure Patients

NCT02624739

COMPLETED NA

CPAP vs ASV for Insomnia

NCT02365064

TERMINATED NA

Cardiovascular Improvements With MV ASV Therapy in Heart Failure

NCT01953874

COMPLETED NA

Effectiveness of Adaptive Servoventilation (ASV) in Patients With Central Sleep Apnea Due to Chronic Opioid Use

NCT01462084

COMPLETED NA

Evaluation of Acclimate Feature for Positive Airway Pressure (PAP) Therapy

NCT01421654

COMPLETED NA

Pediatric Nasal Mask Usability Study

NCT01154322

COMPLETED NA

Complex Sleep Apnea Syndrome (CompSAS) Resolution Study

NCT00915499

COMPLETED NA

GLYCOSA Study:Effect of PAP Treatment on Glycemic Control in Patients With Type 2 Diabetes

NCT00509223

COMPLETED

Validation of the ApneaLink Sleep Screener for Obstructive Sleep Apnea (OSA)

NCT00354614

Phase Distribution

PhaseTrial count
Phase 3 1

What the Pipeline for ResMed Shows

According to the ClinicalTrials.gov registry, ResMed is linked to 25 US clinical trials across every stage of research activity. Of those, 1 studies are currently recruiting, about 4% of the sponsor's indexed portfolio, and 20 are already marked complete, representing roughly 80% of the total.

The phase mix for ResMed reports 1 late-stage studies (Phase 3 and Phase 4 combined) and 0 earlier-phase studies (Phase 1 and Phase 2).

The top therapeutic focus area indexed for ResMed is Obstructive Sleep Apnea with 2 linked trials, and 2 other condition areas appear in the top list above.

How to read these pipeline numbers

Recruiting share is one of the more practical signals here: it reflects how much of a sponsor's research is presently open to new participants, while the completed share indicates the depth of finished work that has already contributed registry results. Both counts come directly from the public ClinicalTrials.gov dataset and are refreshed on the registry side; this page mirrors the latest data pull without altering it.

A portfolio weighted toward Phase 3 usually reflects an organization advancing candidates toward regulatory review, where the research centers on comparative efficacy and broader safety across larger populations. A heavier Phase 1 and Phase 2 tilt generally indicates exploratory work, safety, dosing, and early signal detection, and is common among research-forward sponsors that seed many early programs. Phase 4 entries, when present, track interventions already in real-world use and typically focus on long-term safety, effectiveness across subgroups, or formulation comparisons.

That distribution is a quick read of where the organization concentrates its research attention; it does not imply product availability, market share, or any clinical endorsement. All numbers on this page come from ClinicalTrials.gov maintained by the National Library of Medicine, and counts can shift as new studies are registered or existing ones update their status. This information is provided for reference and educational purposes only, not as medical, investment, or regulatory advice, verify current details directly with ClinicalTrials.gov before relying on any figure here.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page aggregates every registered trial from this sponsor, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.