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Combined Use of Radiofrequency-ablation and Balloon-septostomy in the Creation of a Stable Inter-atrial Communication (CURB)

N

National Center for Cardiovascular Diseases

Status

Enrolling

Conditions

Pulmonary Arterial Hypertension

Treatments

Other: Radiofrequency catheter ablation
Other: Balloon atrial septostomy

Study type

Interventional

Funder types

Other

Identifiers

NCT03554330
2017-GZ15

Details and patient eligibility

About

Though graded balloon-atrial-septostomy (BAS) has been accepted as an effective palliative therapy for severe pulmonary arterial hypertension, spontaneous closure of septostomy is not uncommon. Radiofrequency-catheter-ablation (RFA), which has the potential to cause irreversible damage around the rim of created inter-atrial communication, might contribute to prevent the spontaneous closure. In patients with severe pulmonary arterial hypertension, the combined use of RFA and BAS (CURB) is investigated to create a stable inter-atrial communication.

Full description

Balloon atrial septostomy (BAS) is an important palliative therapy in patients with refractory pulmonary arterial hypertension. However, the incidence of spontaneous closure is higher, which limits the clinical utilization of this procedure. Radiofrequency catheter ablation (RFA) has the potential to cause irreversible damage around the rim of fenestration created with BAS, which might prevent the re-adhesion of the septal remnants. In addition, RFA on fossae ovalis might reduce the elastic recoil of local tissue and contribute to create larger inter-atrial fenestration with same BAS procedure. In this study, the patients between 18 and 60 years of age who have severe pulmonary arterial hypertension associated with right heart failure refractory to medical therapy or severe syncopal symptoms may be eligible for this study (idiopathic severe pulmonary arterial hypertension or severe pulmonary arterial hypertension associated with repaired congenital heart disease). These patients will be randomized 1:1:1 to control group, single-RFA group and double-RFA group:

  1. In control group: only BAS is carried out.
  2. In single-RFA group: after BAS procedure identical to control group, RFA is performed immediately around the rim of created inter-atrial fenestration.
  3. In double-RFA group: the first step is RFA on fossae ovalis; and then the other two steps are identical to the single-RFA group (BAS and RFA around the rim of fenestration).

The immediate size of created fenestration will be determined with intra-cardiac echocardiography, and the patency and size of fenestration will be followed up for 12 months. During the period of follow up, the other evaluations will include the exercise tolerance, cardiac index, systemic arterial oxygen saturation and so on.

Enrollment

90 estimated patients

Sex

All

Ages

18 to 60 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Idiopathic severe pulmonary arterial hypertension;
  2. Severe pulmonary arterial hypertension associated with repaired congenital heart disease;
  3. World Health Organization functional class III or IV with right heart failure refractory to medical therapy;
  4. Severe syncopal symptoms;

Exclusion criteria

  1. Mean right atrial pressure >20 mm Hg;
  2. Room-air resting arterial oxygen saturation <85%;
  3. Left ventricular end diastolic pressure (LVEDP) >18mm Hg;
  4. Pulmonary vascular resistance >55 wood units/m2.
  5. Severe right ventricular failure on cardio-respiratory support
  6. The predicted one-year survival <40%;

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

90 participants in 3 patient groups

control group
Active Comparator group
Description:
Only graded balloon atrial septostomy is carried out, and no radiofrequency catheter ablation is performed.
Treatment:
Other: Balloon atrial septostomy
single-RFA group
Experimental group
Description:
After graded balloon atrial septostomy procedure identical to control group, radiofrequency catheter ablation will be performed immediately around the rim of created inter-atrial fenestration.
Treatment:
Other: Radiofrequency catheter ablation
Other: Balloon atrial septostomy
double-RFA group
Experimental group
Description:
The first step is radiofrequency catheter ablation on fossae ovalis; and then the other two steps are identical to the single-RFA group (graded balloon atrial septostomy and radiofrequency catheter ablation around the rim of fenestration).
Treatment:
Other: Radiofrequency catheter ablation
Other: Balloon atrial septostomy

Trial contacts and locations

1

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Central trial contact

Chaowu Yan, PhD and MD

Data sourced from clinicaltrials.gov

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