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PADN to Treat Severe Obstructive Sleep Apnea

Not Applicable
Terminated
Conditions
Obstructive Sleep Apnea Syndrome
Interventions
Procedure: Sham procedure
Procedure: Pulmonary Arterial Denervation
Registration Number
NCT02687477
Lead Sponsor
Nanjing First Hospital, Nanjing Medical University
Brief Summary

This project is focused on the treatment of severe obstructive sleep apnea with pulmonary artery denervation (PADN). Although it has now been proved that continuous positive airway pressure (CPAP) is the primary treatment for obstructive sleep apnea, on the other hand, there is evidence that 25 to 50% of patients can not tolerate CPAP.

The investigators previously reported the safety and efficacy of pulmonary artery denervation (PADN) for treatment of pulmonary hypertension. Excessive sympathetic activation play an important role in the occurrence and development of OSA and cause cardiovascular events. It is worth evaluating the feasibility and tolerance of introducing PADN at the severe stage of obstructive sleep apnea. Therefore, the purpose of our study is to evaluate the safety and feasibility of PADN in the treatment of severe OSA.

Detailed Description

Not available

Recruitment & Eligibility

Status
TERMINATED
Sex
All
Target Recruitment
1
Inclusion Criteria
  • Apnea hypopnea index more than 30, not tolerated or refused continuous positive airway pressure;
Exclusion Criteria
  • Acute coronary syndrome;
  • Pregnant;
  • Expected life less than 12 months;

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Sham procedureSham procedurePatients in the sham group will take sham procedure like PADN.
Pulmonary Arterial DenervationPulmonary Arterial DenervationContrast pulmonary artery (PA) angiography was performed to localize the pulmonary artery bifurcation level and calculate the PA diameter.Once the anatomy was deemed acceptable, the radiofrequency ablation catheter was introduced into the distal bifurcation area of the main PA.This was then maneuvered within the PA to allow energy delivery to ensure that the electrodes were tightly in contact with the endovascular surface. About two to three ablations at 1-15 W for 240 seconds each point were performed in the distal bifurcation area of the main PA.
Primary Outcome Measures
NameTimeMethod
the change from baseline to month 6 in apnea-hypopnea indexBaseline and 6 months
Secondary Outcome Measures
NameTimeMethod
the absolute change in Epworth Sleepiness Scale from baseline to follow-upBaseline and 6 months

Trial Locations

Locations (1)

Nanjing First Hospital

🇨🇳

Nanjing, Jiangsu, China

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