Study of Human Botulism Immunoglobulin in Infants With Botulism - Full Text View

Study of Human Botulism Immunoglobulin in Infants With Botulism

This study is currently recruiting participants.
Verified by FDA Office of Orphan Products Development, March 2000

Sponsors and Collaborators:	FDA Office of Orphan Products Development California Department of Health Services
Information provided by:	FDA Office of Orphan Products Development
ClinicalTrials.gov Identifier:	NCT00004401

Purpose

OBJECTIVES: I. Determine the safety of human botulism immune globulin (BIG) in patients with infant botulism by monitoring side effects (e.g., rash, fever, hypotension, and anaphylaxis).

II. Assess the efficacy of BIG in these patients by monitoring disease severity, incidence of complications (respiratory arrest, aspiration, pneumonia, etc.), and length of hospital stay.

Condition	Intervention
Infant Botulism Botulism	Drug: botulism immune globulin

MedlinePlus related topics:

Botulism

Drug Information available for:

Immunoglobulins Globulin, Immune

U.S. FDA Resources

Study Type:	Interventional
Study Design:	Treatment, Open Label

Further study details as provided by FDA Office of Orphan Products Development:

Estimated Enrollment:	120
Study Start Date:	January 1998

Detailed Description:

PROTOCOL OUTLINE: This is an open label, multicenter study. Patients should begin therapy within 72 hours of hospital admission, but may receive human botulism immunoglobulin (BIG) in certain circumstances after 72 hours. Patients receive (BIG) IV. Patients are monitored for side effects, disease severity, complications, and length of hospital stay.

Patients are followed at 2 weeks after treatment, then every 4 weeks for 6 months.

Eligibility

Ages Eligible for Study:	up to 1 Year
Genders Eligible for Study:	Both
Accepts Healthy Volunteers:	No

Criteria

PROTOCOL ENTRY CRITERIA:

--Disease Characteristics--

Clinical diagnosis of infant botulism in previously healthy infant
Bulbar palsies
Constipated Lethargy
Diminished head control
Poor feeding
Generalized weakness and hypotonia
Weak cry
Afebrile (unless secondary infection present)
Subacute to acute onset
Normal electrolytes
Any patient eligible provided no treatment available for life-threatening condition

Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00004401

Locations


United States, California
	California Department of Health Services	Recruiting
	Berkeley, California, United States, 94704-1011
	Contact: Stephen S. Arnon 510-540-2646

Sponsors and Collaborators

FDA Office of Orphan Products Development

California Department of Health Services

Investigators


Study Chair:	Stephen S. Arnon	California Department of Health Services

More Information

Study ID Numbers:	199/13253, CDHS-FDU000476
First Received:	October 18, 1999
Last Updated:	June 23, 2005
ClinicalTrials.gov Identifier:	NCT00004401
Health Authority:	United States: Federal Government

Keywords provided by FDA Office of Orphan Products Development:

bacterial infection

clostridium infection

immunologic disorders and infectious disorders

infant botulism

rare disease

Study placed in the following topic categories:

Bacterial Infections

Gram-Positive Bacterial Infections

Neurotoxicity Syndromes

Neuromuscular Diseases

Botulism

Neurotoxicity syndromes

Poisoning

Rare Diseases

Disorders of Environmental Origin

Clostridium Infections

Immunoglobulins

Additional relevant MeSH terms:

Immunologic Factors

Physiological Effects of Drugs

Food Poisoning

Nervous System Diseases

Neuromuscular Junction Diseases

Pharmacologic Actions

ClinicalTrials.gov processed this record on November 20, 2008