Abstract | OBJECTIVE: METHODS: A double-blind, randomized, placebo-controlled parallel-group study was conducted in 53 patients with primary varicose veins. Patients received either a fixed combination of 3 mg dihydroergotamine and 300 mg troxerutin three times a day or placebo for 3 weeks. Symptomatic improvement was assessed by a self-assessment score, venocontracting effects on a varicose vein were quantified by the venous compliance technique (VCT), and changes in venous dysfunction were measured by digital photoplethysmography ( DPPG). RESULTS: A significant reduction (p < 0.01) of subjective symptoms was observed in both groups. Results from VCT and DPPG after the therapy with dihydroergotamine and troxerutin or placebo were not significantly different (p > 0.05) from pretreatment values. Furthermore, no significant intergroup difference was observed when the before- and after- therapy differences of values of the self-assessment scores (VCT and DPPG) were compared. CONCLUSION:
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Authors | S Schuller-Petrovic, M Wolzt, K Böhler, B Jilma, H G Eichler |
Journal | Clinical pharmacology and therapeutics
(Clin Pharmacol Ther)
Vol. 56
Issue 4
Pg. 452-9
(Oct 1994)
ISSN: 0009-9236 [Print] United States |
PMID | 7955807
(Publication Type: Clinical Trial, Journal Article, Randomized Controlled Trial, Research Support, Non-U.S. Gov't)
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Chemical References |
- Hydroxyethylrutoside
- Vasoconstrictor Agents
- Dihydroergotamine
- troxerutin
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Topics |
- Adult
- Dihydroergotamine
(administration & dosage)
- Double-Blind Method
- Drug Therapy, Combination
- Female
- Humans
- Hydroxyethylrutoside
(administration & dosage, analogs & derivatives)
- Male
- Middle Aged
- Photoplethysmography
(methods)
- Time Factors
- Varicose Veins
(drug therapy, physiopathology)
- Vasoconstrictor Agents
(administration & dosage)
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