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Remote Ischemic Conditioning in Necrotizing Enterocolitis

Remote Ischemic Conditioning in Necrotizing Enterocolitis: Feasibility and Safety Pilot Study.

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03860701
Enrollment
15
Registered
2019-03-04
Start date
2018-12-17
Completion date
2019-08-20
Last updated
2020-10-22

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

Conditions

Enterocolitis, Necrotizing

Brief summary

Necrotizing enterocolitis (NEC) affects up to 10% of very preterm infants. NEC mortality is high (30-50 %) and has remained unchanged over the last decades. New treatments are urgently needed. NEC pathogenesis is multifactorial, but bowel ischemia plays an essential role in NEC development. Remote ischemic conditioning (RIC) consists in inducing brief periods of non-lethal ischemia in a limb distant to an organ suffering from ischemia. RIC has been used in adults, children and term neonates with a variety of diagnosis. However, no study has been done including preterm infants with NEC.

Detailed description

An appropriately sized blood pressure cuff will be applied to an arm or leg and inflated to promote RIC. This study will be conducted in three phases to assess the feasibility and safety of RIC in relation to duration of ischemia time, number of cycles of RIC and whether it is feasible and safe to perform RIC on consecutive days.

Interventions

PROCEDURERemote ischemic conditioning

An appropriately sized blood pressure cuff will be inflated around a limb (systolic blood pressure + 15 mmHg) for different periods of time (1 to up to 4 minutes), times (1 to up to 4 times) and consecutive days (1 to up to 2).

Sponsors

Canadian Institutes of Health Research (CIHR)
CollaboratorOTHER_GOV
The Hospital for Sick Children
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
0 Months to 3 Months

Inclusion criteria

* Patients with NEC (stages I-III Bell's Classification) * Weight greater or equal to 750 g. * Gestational age \< 36 weeks. * Patients whose parents consent to participate in the study.

Exclusion criteria

* Patients with major congenital anomalies * No antecedent of limb ischemia/limb thrombotic events. * No antecedent diagnosis of occlusive arterial or venous thrombosis * Hemodynamic instability

Design outcomes

Primary

MeasureTime frameDescription
Limb perfusion after Remote Ischemic Conditioning1 daysLimb perfusion will be assessed before (baseline) and after Remote Ischemic Conditioning (RIC). Limb perfusion will be determined by oxygen saturation using pulse oximetry. RIC will be considered feasible and safe if the procedure is completed as planned with no failure of limb re-perfusion. Failure is defined as no return of limb arterial oxygen saturation to baseline 4 minutes after the ischemic phase (re-perfusion time).

Secondary

MeasureTime frameDescription
Cutaneous injury1 daysDefined as new-onset skin breakdown, bruising, ecchymosis or petechiae.
Persistent pain1 daysPain measured according to the premature infant pain profile (PIPP) scores (range 0-21). Pain scores will be obtained immediately before (baseline) and 6 hours after RIC. Persistent pain will be defined as a PIPP score higher than the baseline score.

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 11, 2026