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NCT06256640: OBMAD

Mandibular Advancement Device (MAD) in Pregnant Women With Obstructive Sleep Apnea (OSA)

Withdrawn NA Last updated 29 January 2025
What this trial tests

NA trial testing Mandibular advancement Device in Obstructive Sleep Apnea of Adult. Withdrawn.

Timeline
1 February 2024
Primary endpoint
1 February 2025
1 February 2025

Quick facts

Lead sponsorHenry Ford Health System
PhaseNA
StatusWithdrawn
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Start date1 February 2024
Primary completion1 February 2025
Estimated completion1 February 2025
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Henry Ford Health System — full company profile →

Who can join

Adults 18 to 40, female only, with Obstructive Sleep Apnea of Adult or Pregnancy Related. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

We propose a single-arm trial to test the patient uptake and preliminary efficacy of MAD in a sample of 10 pregnant women with mild-to-moderate OSA. Study outcomes include patient-reported symptoms and objectively assessed sleep parameters assessed before treatment, during and after 10 weeks of MAD intervention (during pregnancy) and postpartum.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

Verify or expand the search:

Other recruiting trials for Obstructive Sleep Apnea of Adult

Currently open trials in the same condition.

Other Henry Ford Health System trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06256640.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing