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Hemophilia A Study Clinical Trials Facts presented on Clinical Trials Search isn't designed to be a substitute for proven healthcare advice, calls or treatment using a real mD. We aren't mDs. Always confer with your physician on Hemophilia A Study conditions. Clinical Trials Search.org is a website dedicated to listing clinical research studies in human subjects. Hemophilia A Study Clinical research trials and Hemophilia A Study healthcare trials happen in a lot of of localities across the United States of America. A clinical trial or clinical study is a research project with human volunteer subjects. Clinical drug trials and pharmaceutical clinical trials generally measure the potency of new drugs. The aim of the studies / undertakings is to answer particular human medical questions. Clinical trials are a popular manner for doctors, government agencies, and private sector corporations to discover remedies for all kinds of circumstances, such as Hemophilia A Study. Hemophilia A Study Clinical Trials and other clinical trials allow volunteers to get healthcare treatment alternatives before they are available to the general public. Most times the participants receive treatment for without cost, and occasionally they are paid for their time. Sometimes there is a cost for a Hemophilia A Study clinical trial. Human subjects often receive the most effective healthcare possible for their Hemophilia A Study condition. Risks are a reality, nonetheless, and may include more or frequent dr. calls, healthcare hazards (perhaps life-threatening), and/or the treatment being ineffective. Trials are federally governed with rigorous guidelines to protect clinical trials subjects.

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Hemophilia A Study



Hemophilia A Study

For Condition: Hemophilia A
Status: Completed
Sponsor(s): Wyeth-Ayerst Research ,
Synopsis: To identify the causative mutations in previously untreated patients with hemophilia A enrolled in the ReFacto® clinical safety and efficacy study CTN 93-R833-0XX/C9741-28, using two established hemophilia mutation testing laboratories (one in Europe and one in North America).
Details:
Eligibility:
Study Type:
  Interventional, Treatment
Minimum Age/Maximum Age: /
Genders: Both
Protocol Entry Criteria: Inclusion Criteria: - Patients who were or are enrolled in Study CTN 93-R833-0XX/C9741-28, and have been treated with ReFacto® during this study are eligible for participation. - The patient (or legal guardian) must be willing to give written informed consent before any study-related procedures are performed. - A blood sample will be collected from each patient for the purpose of this study and will be analyzed at one or both of the designated central laboratories. Exclusion Criteria: - Any condition which, in the investigator's opinion, places the patient at undue risk.
Total Enrollment: 

Location and Contact Information:


Additional Information:
Study ID Numbers:
  C0007-28/3082A1-302; 
Study Start Date: 
Record last reviewed: June 2002
Additional information available at: clinicaltrials.gov
Clinicaltrials.gov Reference link: NCT00038909

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