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Potts-shunt for the Treatment of Pediatric Patients With Severe Pulmonary Hypertension

Multicenter, Prospective, and Exploratory Study of Potts-shunt for the Treatment of Pediatric Patients With Severe Pulmonary Hypertension

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06429579
Enrollment
120
Registered
2024-05-28
Start date
2024-04-23
Completion date
2029-04-23
Last updated
2024-05-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pulmonary Artery Hypertension

Brief summary

This is a multi-center, perspective, and exploratory study aimed at evaluating the 3-years clinical outcome of Potts-shunt procedure for pediatric patients with severe pulmonary artery hypertension (PAH). The included criteria are as followed: 1)6 months \< age ≤ 18 years; 2) ESC 2022 Group I PAH; 3) Have received standardized drug therapy for at least 6-9 months and still remain at intermediate to high/high-risk status of the criteria of ESC2022; 4) Presenting with significant clinical manifestations (i.e., progressive symptoms/syncope history/growth and development restriction, etc); 5) Informed consent form signed by the patient and their guardian. The excluded criteria are as followed: 1) ESC 2022 Group II-V PAH; 2) Poor right ventricular function: RVEF \< 25% or RVFAC \< 20%; 3) Deteriorated general condition: requiring ICU resuscitation or ECMO assistance; 4) Pulmonary artery pressure/main arterial pressure ratio \< 0.7; 5) Six-minute walk distance \< 150 meters (only applicable to patients aged 8 and above); 6) No significant improvement in RVEF under triple drug therapy. All of the pediatric patients with severe PAH who attend to pediatric cardiac outpatient clinic and meet the designed included criteria and excluded criteria will be enrolled in this study. All of the participants will be divided into two groups (Potts-shunt combined with conventional drug therapy group and only conventional drug therapy group) according to their individual health status (i.e., some contraindications of surgery) and their (or their parents') aspiration for Potts-shunts procedure. Follow-up is designed (eight-times follow-up) at the time of Potts-shunt procedure, post-operative ICU period, one month, three months, six months, one year, two years, and three years after Potts-shunt procedure or the rejection of Potts-shunt procedure. The items of follow-up include state of survival, whether or not have the lung transplantation (LTx), clinical manifestation, laboratory examination, function of right ventricle (detected by echocardiogram and cardiac magnetic resonance imaging), and the pulmonary circulation pressure (detected by right heart catheterization or Swan-Ganz catheterization). Primary outcome is the incidence rates of death or LTx three-years after Potts-shunt. Secondary outcomes are as followed: 1) Number and incidence rate of postoperative complications in patients undergoing Potts-shunt procedure; 2) Three-year WHO cardiac functional and 6-minute walk distance after Potts-shunt procedure; 3) the NT-ProBNP levels three-years after Potts-shunt procedure; 4) Right ventricular function on echocardiography three years after Potts-shunt procedure; 5) Right ventricular function on cardiac magnetic resonance imaging three years after Potts-shunt procedure; 6) Pulmonary circulation pressure measured by right heart catheterization or Swan-Ganz catheterization three years after Potts-shunt procedure; 7) Three-year mortality or LTx incidence rates after only conventional drug therapy.

Interventions

PROCEDUREComprehensive therapy combined Potts-shunt procedure and conventional drug therapy

Potts-shunt procedure is the surgery that connect the descending aorta and the left/main pulmonary artery by direct anastomosis, a Gore-tex tube or a Gore-tex tube with flap.

DRUGOnly conventional drug therapy

Only conventional drug therapy (i.e., Prostacyclin analogues, PDE-5 inhibitors, and Endothelin receptor antagonists)

Sponsors

China National Center for Cardiovascular Diseases
Lead SponsorOTHER_GOV

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
6 Months to 18 Years
Healthy volunteers
No

Inclusion criteria

1. 6 months < age ≤ 18 years; 2. ESC 2022 Group I PAH; 3. Have received standardized drug therapy for at least 6-9 months and still remain at intermediate to high/high-risk status of the criteria of ESC2022; 4. Presenting with significant clinical manifestations (i.e., progressive symptoms/syncope history/growth and development restriction, etc); 5. Informed consent form signed by the patient and their guardian.

Exclusion criteria

1. ESC 2022 Group II-V PAH; 2. Poor right ventricular function: RVEF < 25% or RVFAC < 20%; 3. Deteriorated general condition: requiring ICU resuscitation or ECMO assistance; 4. Pulmonary artery pressure/main arterial pressure ratio < 0.7; 5. Six-minute walk distance < 150 meters (only applicable to patients aged 8 and above); 6. No significant improvement in RVEF under triple drug therapy.

Design outcomes

Primary

MeasureTime frameDescription
Mortality or Lung transplantationFrom the date of enrollment until the date of dear from any cause or lung transplantation, which ever came first, accessed up to 3 yearsThe incidence rates of death or lung transplantation 3 years after Potts-shunt, accessed by in-patient, out-patient, or telephone follow-up

Secondary

MeasureTime frameDescription
World Health Organization functional class (WHO-FC) after Potts-shunt procedureFrom the date of enrollment to the date of every view-point, assessed up to 3 yearsWHO-FC was designed to measure the severity of pulmonary hypertension based on symptoms of dyspnea, fatigue, chest pain, and related syncope, accessed by the pediatric doctors.
NT-ProBNP levels after Potts-shunt procedureFrom the date of enrollment to the date of every view-point, assessed up to 3 yearsNT-ProBNP (pg/ml) accessed by laboratory test
Right ventricular function on cardiac magnetic resonance imaging after Potts-shunt procedureFrom the date of enrollment to the date of every view-point, assessed up to 3 yearsThe RVEF (%) accessed by cardiac MRI
Number and incidence rate of postoperative complications in patients undergoing Potts-shunt procedureFrom the date of enrollment to the date of any postoperative complications, whichever came first, accessed up to 3 yearsPostoperative complications include hemoptysis, syncope, pulmonary hypertension crisis, low blood oxygen in the lower extremities etc. accessed by pediatric ICU doctors.
Pulmonary circulation pressure measured by right heart catheterization or Swan-Ganz catheterization after Potts-shunt procedureFrom the date of enrollment to the date of every view-point, assessed up to 3 yearsSPAP, DPAP, MPAP (mmHg) etc. accessed by right heart catheterization or Swan-Ganz catheterization
Mortality or lung transplantation incidence rates after only conventional drug therapyFrom the date of enrollment until the date of dear from any cause or lung transplantation, which ever came first, accessed up to 3 yearsThe incidence rates of death or lung transplantation 3 years after enrollment
The 6-minutes distance after Potts-shunt procedureFrom the date of enrollment to the date of every view-point, assessed up to 3 yearsThe 6-minutes distance (meter) was designed to measure activity tolerance, accessed by pediatric doctors or parents of participants.
Right ventricular function on echocardiography after Potts-shunt procedureFrom the date of enrollment to the date of every view-point, assessed up to 3 yearsThe RVFAC (%) accessed by echocardiography

Countries

China

Contacts

Primary ContactShoujun Li, MD
drlishoujunfw@163.com+8613501071589

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026