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Nitric Oxide Therapy for Acute Chest Syndrome in Sickle Cell Disease Children

Nitric Oxide Therapy for Acute Chest Syndrome in Sickle Cell Disease Children: Randomized, Double Blind Placebo-controlled Concept-proof Trial

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01089439
Acronym
INNOSTAPED
Enrollment
21
Registered
2010-03-18
Start date
2010-06-30
Completion date
2013-11-30
Last updated
2014-12-04

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

Conditions

Acute Chest Syndrome, Sickle Cell Disease

Keywords

Nitric oxide

Brief summary

Acute chest syndrome is a severe sickle cell disease complication in children requiring blood transfusion therapy to prevent acute respiratory failure and death. Nitric oxide is a potent vasodilator that could reverse pulmonary vascular occlusion and restore normal oxygenation. The randomized trial will test that hypothesis.

Detailed description

Acute chest syndrome is a severe sickle cell disease complication in children requiring blood transfusion therapy to prevent acute respiratory failure and death. Nitric oxide is a potent vasodilator that could reverse pulmonary vascular occlusion and restore normal oxygenation. The randomized trial will test that hypothesis in a prospective randomized double-blind placebo controlled study. 50 children in two years will be included: 25 in each arm.

Interventions

DRUGNitric oxide by inhalation INOMAX

Nitric oxide by inhalation INOMAX 800 ppm 40 ppm during 24 hours then 20 ppm during 24 hours then 10 ppm during 24 hours

DRUGPlacebo

placebo

Sponsors

Mallinckrodt
CollaboratorINDUSTRY
Assistance Publique - Hôpitaux de Paris
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
1 Years to 18 Years
Healthy volunteers
No

Inclusion criteria

* child between 1 and 18 years old * Sickle cell anemia or equivalent (sickle beta 0 thalassemia)whoe weight is between 10kg and 65kg * presenting acute chest syndrome as defined a new radiological infiltrate with tachypnea, respiratory discomfort, cough, chest wall pain and fever more than 38.5°C * hypoxaemia with transcutaneous oxygen saturation equal or less than 92% * informed consent signed by parents and approved by the child able to express his consent * insured by the National social security system or by the universal medical insurance * previous medical physical examination

Exclusion criteria

* respiratory distress with hypoxaemia with transcutaneous oxygen saturation equal or less than 92% under more than 5l/min of oxygen or 40% oxygen inhaled, hypercapnia signs 'sweating, altered consciousness, paCO2 more than 60mmHg) with need of emergency exchange transfusion and/or tracheal intubation with mechanical ventilation * Isolated acute asthmatic crisis * stroke or priapism with emergency acute transfusion needed * acute anemia with hemoglobin drop of more than 20% as compared to steady state hemoglobin * chronic long term transfusion therapy * nitric oxyde hypersensitivity * patients with right-left extra-pulmonary cardiac shunt * patient previously included in the protocol * patient participating in another interventional protocol * pregnancy or breast feeding

Design outcomes

Primary

MeasureTime frame
We will observe the patient's transfusional needs under nitric oxide (MONOXYDE AZOTE) versus placebo inhaled therapy to evaluate inhaled MOXYDE AZOTE efficacy on improving oxygenation (transcutaneous O2 superior to 92% )Oxygenation improvement (transcutaneous O2 superior to 92%) after Gas inhalation will be evaluate 2hours after inclusion and therafter every 2 hours until 12 hours therapy and then every six hours for 3days and then once a day till hospital discharge

Secondary

MeasureTime frame
Number of blood transfusions and total transfused blood volume7 to 10 days
Quantity of Pain-killer drugs required and particularly OPIOIDS7 to 10 days
Duration of Nitric oxide therapyafter 7 to 10 days
Duration of OXYGENOTHERAPY7 to 10 days

Countries

France

Outcome results

None listed

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