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Propofolsleep - A Study on Cardiopulmonary and Pharyngeal Reactions While Drug Induced Sleep Endoscopy (DISE)

NCT03224936 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 20

Last updated 2025-02-14

No results posted yet for this study

Summary

While Drug Induced Sleep Endoscopy (DISE) in patients with obstructive sleep apnea syndrome (OSAS) apnea and hypopnea occur. Because of the induced phases of apnea in a controlled setting it is possible to evaluate the related pathophysiology of apnea. We plan to correlate the Patient State Index (PSI) and other physiologic parameters with phases of apnea and hypopnea.

Conditions

  • Sleep Apnea, Obstructive
  • Electroencephalography
  • Echocardiography
  • Blood Gas Monitoring, Transcutaneous
  • Consciousness Monitors

Interventions

DEVICE

PSI

The PSI delivered by Masimo Root (Sedline) will be measured in all patients.

Sponsors & Collaborators

  • Charite University, Berlin, Germany

    lead OTHER

Principal Investigators

  • Sascha Treskatsch, MD, Prof · Charite University, Berlin, Germany

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-08-22
Primary Completion
2019-10-30
Completion
2019-12-31

Countries

  • Germany

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03224936 on ClinicalTrials.gov