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Carbon Dioxide (Carbogen) for the Treatment of Febrile Seizures

Carbon Dioxide (Carbogen) for the Treatment of Febrile Seizures

Status
Terminated
Phases
Phase 2Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01370044
Acronym
CARDIF
Enrollment
96
Registered
2011-06-09
Start date
2012-08-31
Completion date
2015-06-30
Last updated
2018-01-26

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

Conditions

Febrile Seizure

Keywords

Febrile Seizure, Carbon Dioxide, Carbogen, Respiratory Alkalosis

Brief summary

The aim of this clinical trail is to evaluate the efficacy of a Carbogen inhalation in patients with febrile seizures compared to a placebo-inhalation. Further aims are the evaluation of the safety of the Carbogen inhalation via a low-pressure can with a breathing mask in a home-setting, the manageability of the Carbogen inhalation via a low pressure can with a breathing mask in a home-setting or on the way (mobility), the quality of life of the parents and children using the low pressure can with a breathing mask in a home-setting or on the way (mobility) and the contentment and anxiety of the parents.

Detailed description

For detailed protocol see: Ohlraun S, Wollersheim T, Weiß C, Martus P, Weber-Carstens S, Schmitz D, Schuelke M. CARbon DIoxide for the treatment of Febrile seizures: rationale, feasibility, and design of the CARDIF-study. J Transl Med. 2013 Jun 27;11:157. doi: 10.1186/1479-5876-11-157. BACKGROUND: 2-8% of all children aged between 6 months and 5 years have febrile seizures. Often these seizures cease spontaneously, however depending on different national guidelines, 20-40% of the patients would need therapeutic intervention. For seizures longer than 3-5 minutes application of rectal diazepam, buccal midazolam or sublingual lorazepam is recommended. Benzodiazepines may be ineffective in some patients or cause prolonged sedation and fatigue. Preclinical investigations in a rat model provided evidence that febrile seizures may be triggered by respiratory alkalosis, which was subsequently confirmed by a retrospective clinical observation. Further, individual therapeutic interventions demonstrated that a pCO2-elevation via re-breathing or inhalation of 5% CO2 instantly stopped the febrile seizures. Here, we present the protocol for an interventional clinical trial to test the hypothesis that the application of 5% CO2 is effective and safe to suppress febrile seizures in children. METHODS: The CARDIF (CARbon DIoxide against Febrile seizures) trial is a monocentric, prospective, double-blind, placebo-controlled, randomized study. A total of 288 patients with a life history of at least one febrile seizure will be randomized to receive either carbogen (5% CO2 plus 95% O2) or placebo (100% O2). As recurrences of febrile seizures mainly occur at home, the study medication will be administered by the parents through a low-pressure can fitted with a respiratory mask. The primary outcome measure is the efficacy of carbogen to interrupt febrile seizures. As secondary outcome parameters we assess safety, practicability to use the can, quality of life, contentedness, anxiousness and mobility of the parents. PROSPECT: The CARDIF trial has the potential to develop a new therapy for the suppression of febrile seizures by redressing the normal physiological state. This would offer an alternative to the currently suggested treatment with benzodiazepines. This study is an example of academic translational research from the study of animal physiology to a new therapy. TRIAL REGISTRATION: ClinicalTrials.gov identifier: NCT01370044. DOI: 10.1186/1479-5876-11-157 PMCID: PMC3700755 PMID: 23806032 \[Indexed for MEDLINE\]

Interventions

3 minutes administration of carbogen

DRUGPlacebo

3 minutes administration of oxygen

Sponsors

Charite University, Berlin, Germany
Lead SponsorOTHER

Study design

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

Eligibility

Sex/Gender
ALL
Age
12 Months to 5 Years
Healthy volunteers
No

Inclusion criteria

* condition after febrile seizure * age 12 months to 5 years * written informed consent

Exclusion criteria

* severe other organic disease * meningitis as possible cause for the cerebral seizure * neurologic disease or cerebral dysplasia * cerebrale seizures without fever in the medical history * hypersynchronic eeg activity * disorder of the respiratory tract (Asthma e.g.)

Design outcomes

Primary

MeasureTime frameDescription
number of patients which need Diazepam3 minutesefficacy of a Carbogen inhalation in patients with febrile seizures compared to a placebo inhalation

Secondary

MeasureTime frameDescription
number of severe adverse events3 minutessafety of the Carbogen inhalation via a low-pressure can with a breathing mask in a home-setting
manageability of the application assessed by the parents3 minutesmanageability of the Carbogen inhalation via a low pressure can with a breathing mask in a home-setting or on the way (mobility)
changes in quality of life of the parents and children after use of study medication3 minutesquality of life of the parents and children using the low pressure can with a breathing mask in a home-setting or on the way (mobility)
contentment and anxiety of the parents10 minutesstructured interview of the parents after a seizure

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 23, 2026