Abstract | BACKGROUND: METHODS AND RESULTS: According to a double-blind, randomized, placebo-controlled trial, 29 patients with stable exercise-induced angina pectoris and angiographically proven coronary artery disease received a single daily subcutaneous injection of Parnaparin or placebo on top of aspirin and conventional antianginal medication over 3 months. Patients randomized to Parnaparin showed a significant decrease in the fibrinogen level (P = .035) and an improvement in both the time to 1-mm ST segment depression (P = .008) and the peak ST segment depression (P = .015). The Canadian Cardiovascular Society class for angina pectoris was also improved by Parnaparin (P = .016). Parnaparin did not affect ADP and collagen-induced platelet aggregation, whereas thrombin-induced aggregation was reduced (P = .0001). The bleeding time was slightly prolonged, but this was not associated with any significant bleeding. CONCLUSIONS:
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Authors | G Melandri, F Semprini, V Cervi, N Candiotti, E Palazzini, A Branzi, B Magnani |
Journal | Circulation
(Circulation)
Vol. 88
Issue 6
Pg. 2517-23
(Dec 1993)
ISSN: 0009-7322 [Print] United States |
PMID | 8252662
(Publication Type: Clinical Trial, Journal Article, Randomized Controlled Trial)
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Chemical References |
- Cardiovascular Agents
- Heparin, Low-Molecular-Weight
- Fibrinogen
- parnaparin
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Topics |
- Adult
- Aged
- Angina Pectoris
(blood, drug therapy, physiopathology)
- Bleeding Time
- Cardiovascular Agents
(administration & dosage)
- Double-Blind Method
- Drug Therapy, Combination
- Exercise Test
- Female
- Fibrinogen
(metabolism)
- Heparin, Low-Molecular-Weight
(administration & dosage)
- Humans
- In Vitro Techniques
- Male
- Middle Aged
- Platelet Aggregation
(drug effects)
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