Ignite Creation Date:
2024-05-06 @ 10:33 AM
Last Modification Date:
2024-10-26 @ 12:31 PM
Study NCT ID:
NCT03282266
Status:
COMPLETED
Last Update Posted:
2022-03-29
First Post:
2017-09-12
Brief Title:
Safety and Efficacy of Pulmonary Artery Denervation in Patients With Pulmonary Arterial Hypertension
Sponsor:
Nanjing First Hospital Nanjing Medical University
Organization:
Nanjing First Hospital Nanjing Medical University
Study Overview
Official Title:
A Randomised Single-blind Sham Operation-controlled Study to Evaluate the Safety and Efficacy of the Pulmonary Artery Denervation for the Treatment of Pulmonary Arterial Hypertension
Status:
COMPLETED
Status Verified Date:
2022-03
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
PADN-CFDA
Brief Summary:
The objective of this randomized control trial is to gain clinical insight on the use of pulmonary artery denervation PADN for the treatment of pulmonary arterial hypertension PAH The primary objective is to assess effectiveness and safety of PADN for the treatment of PAH
Detailed Description:
The current study is designed as a multicenter randomized and prospective study aiming to compare the change in 6-minute walk distance 6MWD of PADN on PAH patients Based on the previous studies the 6MWD was 1324 m after 6-month treatment using target drugs And our previous data showed that 6MWD at 6-month after PADN procedure was 6585 m As a result a total of 128 patients with Group I PAH are randomized at a ratio of 11 to either PADN procedure plus phosphodiesterase-5 inhibitors PDE5i group PADN group or sham-PADN procedure plus PDE5i group Sham group using a randomization schedule blocked by site The combination therapy of PDE5i with additional other PAH-specific target drugs is not recommended for all patients and is left at physicians discretion in both groups
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
False
Is an FDA AA801 Violation?:
None