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Search / Trial NCT07039604

Real-World Study of PADN for the Treatment of PAH

Launched by PULNOVO MEDICAL (WUXI) CO., LTD. · Jun 17, 2025

Trial Information

Current as of July 22, 2025

Recruiting

Keywords

ClinConnect Summary

This clinical trial is studying a treatment called Pulmonary Artery Denervation (PADN) for people with Pulmonary Arterial Hypertension (PAH), a condition where high blood pressure affects the arteries in the lungs. The study is looking at how well this treatment works in real-life settings for patients who have already had the PADN procedure since March 2024.

If you have been diagnosed with PAH and have had the PADN treatment recently, you might be eligible to join. Participants need to be able to give permission for their health information to be used and must be willing to follow the treatment and attend follow-up visits. There are no specific age or gender restrictions, and no other major exclusions. Being part of the study means your health will be monitored to better understand how effective and safe PADN is for treating PAH outside of a clinical trial setting.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • 1. Diagnosed with PAH and received PADN procedure since March 2024.
  • 2. No contraindications to procedure.
  • 3. Able to provide informed consent and authorize use of health/research data.
  • 4. Compliant with treatment and follow-up requirements.
  • Exclusion Criteria:
  • None specified.

About Pulnovo Medical (Wuxi) Co., Ltd.

Pulnovo Medical (Wuxi) Co., Ltd. is a leading medical technology company specializing in innovative solutions for cardiovascular and respiratory care. With a focus on developing advanced medical devices, Pulnovo is dedicated to enhancing patient outcomes through cutting-edge research and clinical trials. The company leverages a robust team of experts and state-of-the-art facilities to drive innovation in the healthcare sector, ensuring the delivery of safe and effective treatments. As a clinical trial sponsor, Pulnovo Medical is committed to adhering to the highest regulatory standards, fostering collaboration with clinical partners, and prioritizing patient safety and ethical considerations in all its research endeavors.

Locations

Nanjing, Jiangsu, China

Patients applied

0 patients applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported