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1.
Z Hautkr ; 61(5): 294, 297-304, 1986 Mar 01.
Article in German | MEDLINE | ID: mdl-3962411

ABSTRACT

Treatment with diflorasone diacetate ointment and cream (0.05%) was strikingly successful in a multicenter clinical trial involving 4,651 patients in total suffering from various corticosteroid-sensitive dermatoses. According to the clinical evaluation, 93% of the patients were cured or much improved. Approximately 7% of the patients questioned rated the local tolerance of the two forms of administration as good to very good. Only 4% of the patients rated the tolerance of the ointment or cream as moderate or bad. None of the patients showed any systemic side-effects. The molecular structure of diflorasone-17,21-diacetate and the specific pharmaceutical properties of the ointment and cream evidently guarantee a good bioavailability of the glucocorticosteroid in the skin. Clinical and experimental results confirm that diflorasone diacetate belongs to the group of highly active corticosteroids.


Subject(s)
Betamethasone/analogs & derivatives , Dermatitis/drug therapy , Administration, Topical , Adolescent , Adult , Aged , Betamethasone/adverse effects , Betamethasone/therapeutic use , Child , Dermatitis, Atopic/drug therapy , Dermatitis, Contact/drug therapy , Eczema/drug therapy , Female , Humans , Male , Middle Aged , Psoriasis/drug therapy , Skin/drug effects
2.
Z Hautkr ; 59(23): 1623-34, 1984 Dec 01.
Article in German | MEDLINE | ID: mdl-6240840

ABSTRACT

Ten institutions participated in a controlled clinical trial in order to evaluate the efficacy of topical meclocycline and erythromycin in comparison to placebo with regard to papulopustular acne. Both drugs had been incorporated in the same galenic formulation that served as placebo. The vehicle employed in this study guaranteed equally favorable drug relies for both preparations. At the end of the trial, 419 patients could be evaluated for efficacy. As impartial criterion for evaluation, the number of inflammatory lesions on the right side of the face was counted before and after three months of treatment. In addition, we recorded the patients' and physicians' overall judgment at the end of the study. As compared with placebo, meclocycline as well as erythromycin brought about statistically significant improvement already after two months of treatment. After three months, the results were statistically very highly significant (p less than 0.001). At any time of the study, there could not be demonstrated any difference between the two groups treated with meclocycline and erythromycin.


Subject(s)
Acne Vulgaris/drug therapy , Erythromycin/therapeutic use , Oxytetracycline/analogs & derivatives , Administration, Topical , Chemical Phenomena , Chemistry , Clinical Trials as Topic , Double-Blind Method , Erythromycin/administration & dosage , Humans , Oxytetracycline/administration & dosage , Oxytetracycline/therapeutic use , Suppuration
4.
Z Hautkr ; 58(6): 398-409, 1983 Mar 15.
Article in German | MEDLINE | ID: mdl-6342288

ABSTRACT

In a double-blind controlled trial, we have compared the therapeutic effectiveness of Diflorason-Diacetate and Clobetasol-17-propionate with 50 PUVA-resistent psoriatics. Both externals resulted in a highly significant decline of psoriatic symptoms. The difference in therapeutic achievement between the two respective groups was statistically not significant. According to the physician's overall judgement, however, Clobetasol was favored significantly over Diflorasone-Diacetate, while the patients only showed a slight preference for Clobetasol. Based on these findings and previously published results, Diflorasone-Diacetate may be classified as one of the most effective skin corticosteroids, ranging just behind Clobetasol.


Subject(s)
Betamethasone/analogs & derivatives , Clobetasol/analogs & derivatives , PUVA Therapy , Photochemotherapy , Psoriasis/drug therapy , Betamethasone/therapeutic use , Clinical Trials as Topic , Clobetasol/therapeutic use , Double-Blind Method , Humans
5.
J Toxicol Environ Health ; 9(4): 611-8, 1982 Apr.
Article in English | MEDLINE | ID: mdl-6286985

ABSTRACT

Addition of mineral oil to the diet (5%) of two rhesus monkeys that were dosed 29 wk earlier with 2,4,5,2',4',5'-hexabromobiphenyl (HBB) produced a 175% increase in fecal excretion of HBB. A third rhesus monkey was provided with a complete biliary bypass, which permitted the reintroduction of the monkey's own bile or the introduction of the same amount of exogenous bile, which was obtained from control donor monkeys. This experimental design made it possible to measure the portion of fecal excretion that was due to biliary elimination and the portion that was due to intestinal elimination. The effect of mineral oil and/or cholestyramine (CSA) on biliary and intestinal elimination of HBB in the rhesus monkey was then investigated. The results show that (1) fecal excretion of HBB and/or metabolites is due to both biliary and intestinal elimination; (2) during the first 2 wk after completion of dosing, mineral oil does not influence fecal excretion of HBB significantly; (3) 6-7 wk after completion of dosing, mineral oil enhances fecal excretion of HBB by 50%; (4) 8 wk after the last dose of HBB, 4% CSA in the diet increases fecal excretion of HBB and/or metabolites by about 50%; (5) mineral oil specifically stimulates intestinal elimination of HBB; and (6) combined administration of mineral oil and CSA results in an additive effect.


Subject(s)
Biphenyl Compounds/metabolism , Cholestyramine Resin/pharmacology , Mineral Oil/pharmacology , Polybrominated Biphenyls/metabolism , Animals , Bile/metabolism , Drug Interactions , Feces/analysis , Macaca mulatta , Male , Polybrominated Biphenyls/urine
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