Study of Heparin Prophylaxis of Hereditary Angioedema Exacerbations
heparin
Primary Immunodeficiency Diseases+17
+ Hereditary Complement Deficiency Diseases
+ Cardiovascular Diseases
Treatment Study
Summary
Study start date: January 1, 1994
Actual date on which the first participant was enrolled.PROTOCOL OUTLINE: This is a randomized, double blind, placebo controlled, 3 way crossover study. All patients complete diary cards for the first month of the study in order to determine compliance in providing a daily record of symptoms and medication taken. All compliant patients receive subcutaneously injected heparin twice daily, inhaled heparin daily, or matched saline placebo in a random order. Each of the three drug administration periods lasts 2 months, for a total of 6 months of treatment. Patients who have a flare in disease activity that requires hospitalization are terminated from that drug administration period of the study. Patients are followed biweekly during the first month and again at the end of the second month for each of the three 2 month drug administration periods. Completion date provided represents the completion date of the grant per OOPD records
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.24 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Treatment Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.Over 8 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
PROTOCOL ENTRY CRITERIA: --Disease Characteristics-- Confirmed diagnosis of hereditary angioedema (HAE) based upon C4 antigenic level, positive family history, and C1 inhibitor (C1INH) antigenic level (Type I HAE) or functional level (Type II HAE) Functional C1 within normal levels if diagnosis of acquired C1INH is possible Negative family history will not exclude as long as patient meets all other criteria, has normal C1 level, and has no evidence of acquired C1INH deficiency History of symptoms of HAE including episodic swelling, abdominal pain, and/or respiratory difficulty Experiencing a minimum of 1-2 HAE episodes within 6 weeks --Prior/Concurrent Therapy-- Endocrine therapy: Anabolic steroids allowed as long as dose has not been changed in at least 30 days Other: No concurrent and at least 1 week since prior aspirin, nonsteroidal antiinflammatory agents, dipyridamole, Coumadin-like drugs, or any other medication having an effect on coagulation or platelets --Patient Characteristics-- Hematopoietic: No clinically significant history of hematologic disease Hepatic: No clinically significant history of hepatic disease Renal: No clinically significant history of renal disease Cardiovascular: No clinically significant history of cardiac disease or hypertension Pulmonary: No clinically significant history of pulmonary disease Other: No contraindication to the use of inhaled or subcutaneous heparin No drug allergy that would interfere with the study No clinically significant history of: Malignancy Diabetes mellitus Neurologic disease Immunologic disease Bleeding disorder Infirmity No history of drug abuse, alcoholism, psychosis, or other psychological/psychiatric disorder