OCT Evaluates the Effects of CTEPH Treated by Scoring Balloon

Sponsor
First Affiliated Hospital of Chongqing Medical University (Other)
Overall Status
Recruiting
CT.gov ID
NCT05480137
Collaborator
(none)
46
1
2
36
1.3

Study Details

Study Description

Brief Summary

Chronic thromboembolic pulmonary hypertension (CTEPH) is a disease of obstructive pulmonary artery remodelling as a consequence of major vessel thromboembolism.

The diagnosis of CTEPH is based on findings obtained after at least 3 months of effective anticoagulation in order to discriminate this condition from subacute PE. These findings are mean pulmonary artery pressure ≥25mmHg with pulmonary artery wedge pressure ≤15 mmHg, mismatched perfusion defects on lung scan and specific diagnostic signs for CTEPH seen by multidetector CT angiography, MR imaging or conventional pulmonary cineangiography, such as ring-like stenoses, webs/slits and chronic total occlusions (pouch lesions or tapered lesions). Balloon pulmonary angioplasty (BPA) is a type of effective treatment for CTEPH. Plain balloon is usually used in BPA surgery,however,the efficacy and safety of NSE scoring balloon in BPA is not clear. Optical coherence tomography(OCT)as a good assessment methods has been reported. Our study aims to explore the efficacy and safty of NSE scoring balloon based on OCT in BPA .

Condition or Disease Intervention/Treatment Phase
  • Procedure: NSE scoring balloon and plain balloon angioplasty
N/A

Detailed Description

After right heart catheterization,BPA procedures are performed via femoral vein approach. 8-Fr sheath is inserted into the vein and 6-Fr guiding cathater was advanced to the main pulmonary artery through the 8-Fr guiding catheter using a 0.035-inch wire. We select a branch of the pulmonary artery by a 6-Fr guiding catheter (JR4.0). Pulmonary angiography is performed manually using half contrast medium diluted with saline. A 0.014-inch guidewire (Sion) is crossed under the pulmonary angiography, and OCT (Fig.1: Types of lesions) is used for the detection of Lumen diameter (mm), Intimal thickness (mm), Intimal area (mm2), Intimal thickness/lumen diameter, Intimal area/lumen area, which are defined as short diameter assessed by OCT. The balloon size, the expansion pressure and the choice of scoring balloon or plain balloon angioplasty are at the discretion of the operator. Balloon-to-vessel (B/V) ratio is defined as the balloon diameter divided by vessel diameter assessed with OCT (1:0.7-1). Pulmonary arteries with an inner diameter of less than 4mm detected by OCT were selected for BPA performance. Scoring balloon and plain balloon are used in half of pulmonary lesions respectively., use the Plain balloon was used to predilate, If the vascular Lesion is a completely occlusive or the scoring balloon cannot pass through vessels.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
46 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Care Provider, Investigator)
Primary Purpose:
Treatment
Official Title:
The Efficacy of Scoring Balloon Angioplasty in the Treatment of Chronic Thromboembolic Pulmonary Hypertension Based on Optical Coherence Tomography:A Single-center Randomized Controlled
Actual Study Start Date :
Aug 30, 2020
Anticipated Primary Completion Date :
Aug 31, 2022
Anticipated Study Completion Date :
Aug 31, 2023

Arms and Interventions

Arm Intervention/Treatment
Other: plain balloon

plain balloon is used in BPA

Procedure: NSE scoring balloon and plain balloon angioplasty
Using NSE scoring balloon or plain balloon in BPA surgery.

Other: NSE scoring balloon

NSE scoring balloon is used in BPA

Procedure: NSE scoring balloon and plain balloon angioplasty
Using NSE scoring balloon or plain balloon in BPA surgery.

Outcome Measures

Primary Outcome Measures

  1. PVR after BPA [1-3 months after BPA]

    Mean pulmonary artery pressure (mPAP), mean pulmonary wedge pressure (mPCWP) and cardiac output (CO) will be combined to report pulmonary vascular resistance (PVR)in Unit Wood. Formula: PVR=(mPAP-mPCWP)/CO

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 80 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. PEA not available in patients with CTEPH

  2. Patients assessed by a multidisciplinary panel as having a large risk-benefit ratio for PEA surgery

  3. Patients with postoperative residual pulmonary hypertension after PEA

  4. Patients with CTEPH not respond well to medical treatment

Exclusion Criteria:
  1. Other cardiovascular diseases, such as Congenital heart disease, valvular disease, cardiomyopathy, aortic dissection, arteritis, arrhythmia, Severe heart failure

  2. Other diseases of the respiratory system, such as chronic obstructive pulmonary disease, asthma, pulmonary bronchial artery embolism, and other diseases, such as vasculitis, Pulmonary sarcoma, etc.

  3. central-type chronic thromboembolic pulmonary hypertension

  4. Other types of PAH except CTEPH

  5. malignant tumor patients

  6. severe renal dysfunction (GFR <30ml/min)

  7. iodine contrast medium allergy

  8. Gravida

  9. high risk of serious bleeding:Active bleeding,Acute stroke,Severe hepatic insufficiency (Child-Pugh C)

Contacts and Locations

Locations

Site City State Country Postal Code
1 the First Affiliated Hospital, Chongqing Medical University Chongqing Chongqing China 400016

Sponsors and Collaborators

  • First Affiliated Hospital of Chongqing Medical University

Investigators

  • Study Chair: Rui Xiang, Phd, First Affiliated Hospital of Chongqing Medical University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Wei Huang, Professor, First Affiliated Hospital of Chongqing Medical University
ClinicalTrials.gov Identifier:
NCT05480137
Other Study ID Numbers:
  • 2022XMSB0000725
First Posted:
Jul 29, 2022
Last Update Posted:
Jul 29, 2022
Last Verified:
Jul 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Jul 29, 2022