Carbon Dioxide (Carbogen) for the Treatment of Febrile Seizures (CARDIF)
Primary Purpose
Febrile Seizure
Status
Terminated
Phase
Phase 2
Locations
Germany
Study Type
Interventional
Intervention
Carbogen
Placebo
Sponsored by
About this trial
This is an interventional treatment trial for Febrile Seizure focused on measuring Febrile Seizure, Carbon Dioxide, Carbogen, Respiratory Alkalosis
Eligibility Criteria
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.)
Sites / Locations
- Charite University Berlin
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Verum
Placebo
Arm Description
Verum arm receiving Carbogen
Placebo arm receiving oxygen
Outcomes
Primary Outcome Measures
number of patients which need Diazepam
efficacy of a Carbogen inhalation in patients with febrile seizures compared to a placebo inhalation
Secondary Outcome Measures
number of severe adverse events
safety of the Carbogen inhalation via a low-pressure can with a breathing mask in a home-setting
manageability of the application assessed by the parents
manageability 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 medication
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)
contentment and anxiety of the parents
structured interview of the parents after a seizure
Full Information
NCT ID
NCT01370044
First Posted
May 20, 2011
Last Updated
January 24, 2018
Sponsor
Charite University, Berlin, Germany
1. Study Identification
Unique Protocol Identification Number
NCT01370044
Brief Title
Carbon Dioxide (Carbogen) for the Treatment of Febrile Seizures
Acronym
CARDIF
Official Title
Carbon Dioxide (Carbogen) for the Treatment of Febrile Seizures
Study Type
Interventional
2. Study Status
Record Verification Date
January 2018
Overall Recruitment Status
Terminated
Why Stopped
results of interim analysis (not safety relevant)
Study Start Date
August 2012 (undefined)
Primary Completion Date
June 2015 (Actual)
Study Completion Date
June 2015 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Charite University, Berlin, Germany
4. Oversight
5. Study Description
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]
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Febrile Seizure
Keywords
Febrile Seizure, Carbon Dioxide, Carbogen, Respiratory Alkalosis
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
96 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Verum
Arm Type
Experimental
Arm Description
Verum arm receiving Carbogen
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Placebo arm receiving oxygen
Intervention Type
Drug
Intervention Name(s)
Carbogen
Other Intervention Name(s)
Low pressure flask with mask containing 6 L carbogen
Intervention Description
3 minutes administration of carbogen
Intervention Type
Drug
Intervention Name(s)
Placebo
Other Intervention Name(s)
Low pressure flask with mask containing 6 L oxygen
Intervention Description
3 minutes administration of oxygen
Primary Outcome Measure Information:
Title
number of patients which need Diazepam
Description
efficacy of a Carbogen inhalation in patients with febrile seizures compared to a placebo inhalation
Time Frame
3 minutes
Secondary Outcome Measure Information:
Title
number of severe adverse events
Description
safety of the Carbogen inhalation via a low-pressure can with a breathing mask in a home-setting
Time Frame
3 minutes
Title
manageability of the application assessed by the parents
Description
manageability of the Carbogen inhalation via a low pressure can with a breathing mask in a home-setting or on the way (mobility)
Time Frame
3 minutes
Title
changes in quality of life of the parents and children after use of study medication
Description
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)
Time Frame
3 minutes
Title
contentment and anxiety of the parents
Description
structured interview of the parents after a seizure
Time Frame
10 minutes
10. Eligibility
Sex
All
Minimum Age & Unit of Time
12 Months
Maximum Age & Unit of Time
5 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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.)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Markus Schülke-Gerstenfeld
Organizational Affiliation
Charite - NeuroCure
Official's Role
Principal Investigator
Facility Information:
Facility Name
Charite University Berlin
City
Berlin
ZIP/Postal Code
10107
Country
Germany
12. IPD Sharing Statement
Citations:
PubMed Identifier
23806032
Citation
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.
Results Reference
background
Links:
URL
https://neurocure.de/ncrc/ueber-uns.html
Description
Homepage of the NeuroCure Clinical Resaerch Center at the Charité Berlin
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Carbon Dioxide (Carbogen) for the Treatment of Febrile Seizures
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