Last updated: March 7, 2017
Sponsor: Drexel University College of Medicine
Overall Status: Completed
Phase
N/A
Condition
Multiple Sclerosis
Scar Tissue
Amyotrophic Lateral Sclerosis (Als)
Treatment
N/AClinical Study ID
NCT00718393
Internal-16964
Ages 20-85 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Diagnosis of definite or probable ALS by the El Escorial Criteria
Participants must be medically able to undergo the study procedures
Subjects must have a registered nurse who can administer the drug daily and alsoinspect the IV site
Not Pregnant
Willing to pay for the cost of drug, administration, and safety testing
Able to give informed consent
Exclusion
Exclusion Criteria:
Patients who are not diagnosed with ALS by a physician
Patients unable to give informed consent
Patients who have a history of sensitivity to cephalosporin or penicillin antibiotics (such as Ancef, Keflex, Ceclor, Ceftin, Lorabid, Suprax, or Fortaz).
Study Design
Total Participants: 1
Study Start date:
June 01, 2007
Estimated Completion Date:
October 31, 2015