Trial record 8 of 18 for:
Open Studies | "Cerebellar Diseases"
Safety and Efficacy of Intravenous Immune Globulin in Treating Spinocerebellar Ataxia
This study is currently recruiting participants.
Verified March 2012 by University of South Florida
Sponsor:
University of South Florida
Collaborator:
Baxter Healthcare Corporation
Information provided by (Responsible Party):
Theresa Zesiewicz, University of South Florida
ClinicalTrials.gov Identifier:
NCT01350440
First received: April 20, 2011
Last updated: March 26, 2012
Last verified: March 2012
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Purpose
This is a preliminary study to determine the safety and efficacy of intravenous immune globulin in treating Spinocerebellar Ataxia. The investigators aim to assess changes in clinical measures of disease severity before and after treatment.
| Condition | Intervention | Phase |
|---|---|---|
|
Spinocerebellar Ataxia Type 3 |
Biological: IVIG |
Phase 2 |
| Study Type: | Interventional |
| Study Design: | Intervention Model: Single Group Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | Safety and Efficacy of Intravenous Immune Globulin in Treating Spinocerebellar Ataxia |
Resource links provided by NLM:
Genetics Home Reference related topics:
autosomal recessive cerebellar ataxia type 1
infantile-onset spinocerebellar ataxia
Marinesco-Sjögren syndrome
spinocerebellar ataxia type 1
spinocerebellar ataxia type 2
spinocerebellar ataxia type 3
spinocerebellar ataxia type 6
VLDLR-associated cerebellar hypoplasia
U.S. FDA Resources
Further study details as provided by University of South Florida:
Primary Outcome Measures:
- Scale for the Assessment and Rating of Ataxia [ Time Frame: participants will be followed for approximately 4 months ] [ Designated as safety issue: No ]
Secondary Outcome Measures:
- Timed 25 foot walk [ Time Frame: participants will be followed for approximately 4 months ] [ Designated as safety issue: No ]
- Clinical Global impression [ Time Frame: participants will be followed for approximately 4 months ] [ Designated as safety issue: No ]
- Biodex Balance SD [ Time Frame: participants will be followed for approximately 4 months ] [ Designated as safety issue: No ]
- Gait Rite Mat [ Time Frame: participants will be followed for approximately 4 months ] [ Designated as safety issue: No ]
- Berg balance scale [ Time Frame: participants will be followed for approximately 4 months ] [ Designated as safety issue: No ]
- Complete Metabolic Panel [ Time Frame: participants will be followed for approximately 4 months ] [ Designated as safety issue: Yes ]
- Complete Blood Count [ Time Frame: participants will be followed for approximately 4 months ] [ Designated as safety issue: Yes ]
| Estimated Enrollment: | 6 |
| Study Start Date: | August 2011 |
| Estimated Study Completion Date: | December 2012 |
| Estimated Primary Completion Date: | December 2012 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: IVIG
Intravenous Immune Globulin
|
Biological: IVIG
Intravenous Immune Globulin
|
Eligibility| Ages Eligible for Study: | 10 Years to 50 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria:
- Outpatients with SCA 3 diagnosed by a movement disorder specialist and confirmed by genetic testing. Three patients with each diagnosis will be enrolled.
- Age 10 years to 50 years.
- Able to ambulate with or without assistance for 30 feet.
- Women of child-bearing potential must use a reliable method of contraception and must provide a negative pregnancy test at entry into the study.
- Serum creatine kinase, complete metabolic panel, complete blood count, liver function tests, renal function tests, platelets and EKG do not reveal clinically significant abnormalities (results obtained from primary care physician and dated within the past 6 months or obtained at screening visit).
- Stable doses of all medications for 30 days prior to study entry and for the duration of the study.
- Stable doses of all antidepressants and vitamins (including internet purchased idebenone) for 30 days prior to study entry and for the duration of the study. Throughout the study, all possible efforts should be made to maintain stable doses of all other medications.
- Subject permission (informed consent).
Exclusion Criteria:
- Any unstable illness that in the investigator's opinion precludes participation in this study.
- Use of any investigational product within the past 30 days.
- Presence of clinically significant cardiac disease (as determined by the investigator based on EKG and echocardiogram results within the past 6 months). Specifically, an ejection fraction <40%, or a prolonged QT interval (>50% of cycle duration) will be excluded. If the investigator notes clinically significant abnormalities on the EKG or echocardiogram, the subject will be eligible IF they provide clearance from a cardiologist.
- Presence of diabetes (as determined by blood glucose labs within the past 6 months).
- Dementia or other psychiatric illness that prevents the subject from giving informed consent (MMSE less than 25).
- Legal incapacity or limited legal capacity.
- Presence of severe renal disease (estimated creatinine clearance <50 mL/min) or hepatic disease (AST or ALT>2x times normal) (as evidenced by labs reported within the past 6 months).
- Clinically significantly abnormal WBC, hemoglobin or platelet count (as evidenced by labs reported within the past 6 months).
- IgA deficiency (evidenced by screening lab evaluations)
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01350440
Contacts
| Contact: Amber Miller, BS | 813-974-5909 | amiller@health.usf.edu |
Locations
| United States, Florida | |
| University of South Florida | Recruiting |
| Tampa, Florida, United States, 33612 | |
| Principal Investigator: Theresa Zesiewicz, MD | |
Sponsors and Collaborators
University of South Florida
Baxter Healthcare Corporation
Investigators
| Principal Investigator: | Theresa Zesiewicz, MD | University of South Florida |
More Information
No publications provided
| Responsible Party: | Theresa Zesiewicz, Professor of Neurology, University of South Florida |
| ClinicalTrials.gov Identifier: | NCT01350440 History of Changes |
| Other Study ID Numbers: | 10 |
| Study First Received: | April 20, 2011 |
| Last Updated: | March 26, 2012 |
| Health Authority: | United States: Food and Drug Administration |
Additional relevant MeSH terms:
|
Cerebellar Diseases Ataxia Machado-Joseph Disease Spinocerebellar Ataxias Spinocerebellar Degenerations Dyskinesias Neurologic Manifestations Nervous System Diseases Signs and Symptoms Cerebellar Ataxia Brain Diseases Central Nervous System Diseases |
Spinal Cord Diseases Heredodegenerative Disorders, Nervous System Neurodegenerative Diseases Genetic Diseases, Inborn Antibodies Immunoglobulins Immunoglobulins, Intravenous Rho(D) Immune Globulin Immunologic Factors Physiological Effects of Drugs Pharmacologic Actions |
ClinicalTrials.gov processed this record on June 17, 2013