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Remote ischemic conditioning for necrotizing enterocolitis of preterm infants

Remote ischemic conditioning for necrotizing enterocolitis of preterm infants: Single center double blind clinical trial

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000036355
Enrollment
Unknown
Registered
2020-08-22
Start date
2021-01-01
Completion date
Unknown
Last updated
2020-09-07

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

Conditions

Necrotizing enterocolitis

Interventions

RIC group:Remote ischemic conditioning
Control group:No RIC intervention

Sponsors

Children's Hospital of Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Gestational age less than 36 weeks; 2. Weight equal or more than 750 g; 3. Infants with NEC stage I according to Modified Bell's Classification (medically treated cases with no need of surgical intervention at time of enrollment); 4. Patients whose parents consent to participate in the study.

Exclusion criteria

Exclusion criteria: 1. Patients with major congenital heart disease (requiring surgical repair); 2. Patients with major congenital anomalies of gastrointestinal system; 3. Hemodynamically unstable patients (defined as neonates who are on > 2 medications to support blood pressure); 4. With antecedent of limb ischemia/limb thrombotic events; 5. With antecedent diagnosis of occlusive arterial or venous thrombosis.

Design outcomes

Primary

MeasureTime frame
Surgical intervention rate;

Secondary

MeasureTime frame
Mortality rate;Duration of parenteral nutrition;Time at reintroduction of enteral feeds;Time to full enteral feeds;Type of operation;Length of small and large intestine resected;Length of retained intestine;Number and type of inotropic support;Type and duration of ventilatory support;Number of recurrent NEC episodes;

Countries

China

Contacts

Public ContactHaitao Zhu

Children's Hospital of Fudan University

zhuhaitaofd@126.com+86 021-64931212

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026