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Device

Modified CPAP for Obstructive Sleep Apnea (3DCPAP Trial)

N/A
Waitlist Available
Led By Chee ChunMin, MD
Research Sponsored by Beth Israel Deaconess Medical Center
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 30 day
Awards & highlights
No Placebo-Only Group

Summary

This is a prospective pilot to investigate the effect of 3D printer customized CPAP masks on the comfort of patients with obstructive sleep apnea.

Eligible Conditions
  • Obstructive Sleep Apnea

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~30 day
This trial's timeline: 3 weeks for screening, Varies for treatment, and 30 day for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Air leak time
Secondary study objectives
Apnea Hypopnea Index
CPAP Inspiratory pressure
CPAP mask leak volume
+1 more

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

1Treatment groups
Experimental Treatment
Group I: Modified CPAPExperimental Treatment1 Intervention
Single arm cohort study of modified mask

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Who is running the clinical trial?

Beth Israel Deaconess Medical CenterLead Sponsor
855 Previous Clinical Trials
12,930,941 Total Patients Enrolled
Chee ChunMin, MDPrincipal InvestigatorBeth Israel Deaconess Medical Center
~3 spots leftby Nov 2025
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