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RecruitingNCT06822400RIFANUpdated Sep 10, 2025

Investigation of Tetralogy of Fallot in Neonates

An interventional study of corrective surgery within 28 days of birth and corrective surgery between 3-6 months of age in Tetralogy of Fallot (TOF), Pulmonary Stenosis and Ventricular Septal Defects (VSD), sponsored by Beijing Anzhen Hospital. Recruiting at 1 site in China. Open to participants aged 1 Minute to 6 Months. Per ClinicalTrials.gov, last updated 2025-09-10.

Sponsored by Beijing Anzhen Hospital · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Started Mar 2025; still recruiting 1 year 7 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
160
Allocation
Randomized
Ages
1 Minute to 6 Months
Sex
All
01

Study summary

Child health serves as the foundation for overall public health, with neonatal mortality recognized globally as a comprehensive indicator of national health standards and societal advancement. The Healthy Children Action Improvement Plan (2021-2025) sets a national target to reduce neonatal mortality in China to below 3.1‰. Congenital heart disease (CHD), the most prevalent congenital defect among neonates, constitutes a significant cause of disability and premature death in the Chinese population. Annually, approximately 70,000-80,000 neonates are born with CHD, among whom nearly 10,000 present with critical congenital heart disease (CCHD). Postnatal manifestations of CCHD often include cyanosis, hypoperfusion, and respiratory distress, with untreated cases resulting in approximately 50% mortality. CCHD is one of the leading causes of infant death.

Tetralogy of Fallot (TOF), the most common form of CCHD, accounts for a substantial proportion of cyanotic congenital heart diseases. It is characterized by four anatomical abnormalities: ventricular septal defect, pulmonary stenosis, overriding aorta, and right ventricular hypertrophy. These structural defects disrupt intracardiac blood flow, reduce arterial oxygen saturation, and result in cyanosis and other related symptoms. Untreated TOF leads to significant health issues early in life, including growth retardation, recurrent hypoxic episodes, heart failure, and increased susceptibility to infections. Long-term survival is markedly reduced, with only a small proportion surviving into adulthood. Thus, surgical intervention is pivotal for improving outcomes in TOF(Tetralogy of Fallot) patients.

Despite advances in medical technology yielding satisfactory early outcomes, long-term prognosis following TOF correction remains a challenge. Historically, surgical strategies emphasized complete relief of right ventricular outflow tract obstruction, often at the expense of pulmonary valve function. Recent studies, however, highlight the critical role of preserving pulmonary valve function in improving long-term outcomes, as pulmonary valve dysfunction is a leading cause of late right ventricular failure and reintervention. Additionally, surgical approaches, whether via atrial or ventricular access, have inherent advantages and limitations, but neither can fully eliminate the risk of postoperative arrhythmias associated with TOF's anatomical complexity and surgical impact. These issues underscore the necessity for further advancements in long-term management strategies.

Surgical correction of TOF in a single-stage procedure has become standard practice, with the timing of surgery progressively shifting to earlier ages-from school age in the 1990s to the current standard of 3-6 months of age. This timing ensures sufficient weight and organ maturity to withstand the complexities of cardiac surgery. However, in clinical practice, significant challenges persist, including: (1) Deterioration during the waiting period, during which patients may experience recurrent hypoxic episodes, inadequate weight gain, and exacerbated pulmonary vascular underdevelopment, thereby complicating definitive surgery and increasing perioperative risk. (2) Developmental delays due to chronic hypoxemia and heart failure, potentially leading to neurological deficits and pulmonary hypertension, adversely affecting cognitive and motor development. Neonatal repair, performed within 28 days of life, may mitigate these challenges by restoring normal circulatory physiology at the earliest possible stage.

International guidelines endorse neonatal TOF repair for capable centers, citing the potential for enhanced clinical benefits and superior prognoses. Clinical observations at our center indicate several advantages of neonatal TOF repair, including reduced intraoperative bleeding, cleaner surgical fields, and better pulmonary vascular development. These benefits may be attributed to the regenerative potential of neonatal myocardial cells and the absence of prolonged pathological circulatory states, which otherwise exacerbate anatomical abnormalities. Early intervention may reduce right ventricular fibrosis and pulmonary vascular pathology, thereby improving long-term outcomes.

With advancements in surgical techniques and perioperative care, neonatal TOF repair has become a routine practice at our center, with over 100 cases performed annually for two consecutive years. This success is supported by an integrated prenatal-to-postnatal care model, establishing a comprehensive treatment framework.

Given this context, the investigators propose a multicenter, randomized controlled trial (RCT) to compare the safety and efficacy of neonatal and infant TOF repair. This study aims to provide high-quality evidence for clinical practice, determine optimal surgical timing, and enhance overall survival rates and quality of life for TOF patients.

02

Conditions studied

  • Tetralogy of Fallot (TOF)
  • Pulmonary Stenosis
  • Ventricular Septal Defects (VSD)
  • Double Outlet Right Ventricle

Keywords

  • Neonatal
  • Infant
  • RCT
  • surgery
03

In context

Tetralogy of Fallot

93 studies on the registry are indexed under Tetralogy of Fallot; 26 are open to participants now.

This study's planned enrollment of 160 is above the median of 51 across 52 interventional studies indexed under Tetralogy of Fallot.

Browse Tetralogy of Fallot studies →

Lead sponsor

Beijing Anzhen Hospital is the lead sponsor of 188 studies on the registry; 100 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
1 Minute to 6 Months
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

Clinical diagnosis of TOF's Disease. Full-term neonates aged ≤28 days. Birth weight of all eligible male or female patients >2.5 kg. All included study participants must be able to give an informed consent

Exclusion criteria

Exclusion Criteria:

Preterm infants . Coexisting complex cardiac anomalies. Severe TOF with pulmonary artery hypoplasia , recurrent hypoxic episodes , or conditions warranting palliative or single-ventricle repair.

Extra-cardiac anomalies, including genetic or chromosomal abnormalities. Neonatal bronchopulmonary dysplasia. Deteriorating conditions in the control group precluding surgery by 3 months of age.

Parental refusal to participate in the clinical trial.

05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Investigator)
Enrollment
160 participants (estimated)

Study arms

  • Active comparator
    intervention group

    Procedure: corrective surgery within 28 days of birth

  • Placebo comparator
    control group

    Procedure: corrective surgery between 3-6 months of age

Interventions

  • Procedurecorrective surgery within 28 days of birth

    Participants will be randomized into two groups with a 1:1 allocation: Intervention Group: Neonates undergoing surgical correction of TOF within 28 days of birth.

  • Procedurecorrective surgery between 3-6 months of age

    Participants will be randomized into two groups with a 1:1 allocation: Control Group: Infants undergoing surgical correction of TOF between 3-6 months of age

06

What researchers measure

Primary outcomes

  1. Incidence of Treatment-Emergent Adverse Events(mortality)

    All-cause mortality within 30 days postoperatively, encompassing cardiovascular and non-cardiovascular causes.

    Time frame: up to 30 days

  2. Rate of re-intervention 12 months after surgery

    Reoperation rate within 12 months postoperatively based on defined criteria, excluding in-hospital reinterventions.

    Time frame: up to 12 months

Secondary outcomes

  1. Perioperative situation

    Perioperative indicators:surgery duration in minutes

    Time frame: during surgery

  2. Perioperative situation

    Perioperative indicators:bypass time in minutes

    Time frame: during surgery

  3. Perioperative situation

    Perioperative indicators:intensive care unit length of stay in hours

    Time frame: up to 720 hours

  4. Perioperative situation

    Perioperative indicators:duration of ventilation in hours

    Time frame: up to 720 hours

  5. Perioperative situation

    Perioperative indicators:hospital length of stay in days

    Time frame: up to 30 days

  6. Surgical complications

    Surgical complications:postoperative ECMO support in hours

    Time frame: up to 720 hours

  7. Surgical complications

    Surgical complications:peritoneal dialysis in hours

    Time frame: up to 720 hours

  8. Cardiac related examination indicators

    Echocardiographic parameter:right ventricular wall thickness in millimeters

    Time frame: through study completion, an average of 3 year

  9. Cardiac related examination indicators

    Echocardiographic parameter:right ventricular outflow tract gradients in mmHg

    Time frame: through study completion, an average of 3 year

  10. Cardiac related examination indicators

    Echocardiographic paramete:pulmonary regurgitation area in cm\^2

    Time frame: through study completion, an average of 3 year

  11. Cardiac related examination indicators

    Echocardiographic parameter:tricuspid regurgitation area in cm\^2

    Time frame: through study completion, an average of 3 year

  12. Follow up indicators

    weight in kilograms

    Time frame: through study completion, an average of 3 year

  13. Follow up indicators

    height in meters

    Time frame: through study completion, an average of 3 year

  14. Follow up indicators

    weight and height will be combined to report BMI in kg/m\^2

    Time frame: through study completion, an average of 3 year

  15. Economic indicators

    hospitalization costs in yuan

    Time frame: up to 30 days

  16. Economic indicators

    operation costs in yuan

    Time frame: during surgery

  17. Economic indicators

    medical costs in yuan during perioperative and postoperative follow-up

    Time frame: through study completion, an average of 3 year

07

Study locations

1 of 1 sites recruiting
  • Beijing Anzhen Hospital
    Beijing, Beijing Municipality 100013, China
    • Qiang Wang MD Beijing Anzhen Hospital,Capital Medical University · Contact · wq.cory@163.com · 8613811548581
    Recruiting
08

References and documents

Individual participant data

Plan to share: Yes

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 10, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06822400
Lead sponsor
Beijing Anzhen Hospital
Collaborators
Children's Hospital of Fudan University, Suzhou University Affiliated Children's Hospital, Shenzhen Children's Hospital, West China Second University Hospital
Responsible party
Sponsor
First posted
Feb 12, 2025
Start date
Mar 1, 2025
Primary completion
Jan 31, 2028 (estimated)
Completion
Jan 31, 2028 (estimated)
Last update
Sep 10, 2025

Study contacts

Qiang Wang Prof Beijing Anzhen Hospital,Capital Medical University
Contact
wq.cory@163.com
8613811548581

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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