{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,28]],"date-time":"2026-10-28T00:01:11Z","timestamp":1793145671973,"version":"4.5.0"},"reference-count":29,"publisher":"Wiley","issue":"7","license":[{"start":{"date-parts":[[2015,6,24]],"date-time":"2015-06-24T00:00:00Z","timestamp":1435104000000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Int J Dermatology"],"published-print":{"date-parts":[[2015,7]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>Cutaneous leishmaniasis (<jats:styled-content style=\"fixed-case\">CL<\/jats:styled-content>) is a major world health problem, which is increasing in incidence. Pentavalent antimonials have been considered as standard treatment for leishmaniasis. Many studies are performed to find an effective and safe treatment for patients with <jats:styled-content style=\"fixed-case\">CL<\/jats:styled-content>. The aim of this study was to compare the effect of oral cimetidine and low\u2010dose systemic meglumine antimoniate (<jats:styled-content style=\"fixed-case\">MA<\/jats:styled-content>) with standard dose of systemic <jats:styled-content style=\"fixed-case\">MA<\/jats:styled-content> in the treatment of <jats:styled-content style=\"fixed-case\">CL<\/jats:styled-content>. This study was, to our knowledge, the first to show the effect of combination therapy oral cimetidine and <jats:styled-content style=\"fixed-case\">MA<\/jats:styled-content> in the treatment of <jats:styled-content style=\"fixed-case\">CL<\/jats:styled-content> all over the world. In this randomized double\u2010blind placebo\u2010controlled clinical trial, 120 patients with suspected <jats:styled-content style=\"fixed-case\">CL<\/jats:styled-content> were referred to the Aleppo University Hospital Clinic; 90 of these patients with the clinical and parasitological diagnosis of <jats:styled-content style=\"fixed-case\">CL<\/jats:styled-content> were recruited and were randomly divided into three treatment groups of 30 subjects each. Group A was treated with <jats:styled-content style=\"fixed-case\">MA<\/jats:styled-content> 60\u00a0mg\/kg\/d <jats:styled-content style=\"fixed-case\">IM<\/jats:styled-content> and oral placebo. Groups B and C received <jats:styled-content style=\"fixed-case\">MA<\/jats:styled-content> 30\u00a0mg\/kg\/d <jats:styled-content style=\"fixed-case\">IM<\/jats:styled-content> and oral cimetidine 1200\u00a0mg\/d, <jats:styled-content style=\"fixed-case\">MA<\/jats:styled-content> 30\u00a0mg\/kg\/d <jats:styled-content style=\"fixed-case\">IM<\/jats:styled-content> and oral placebo, respectively. The duration of treatment was three weeks for all groups. The effectiveness of the treatment was classified in three levels as complete response, partial response, and no response. Data were analyzed by <jats:styled-content style=\"fixed-case\">SPSS<\/jats:styled-content> 19 using <jats:styled-content style=\"fixed-case\">KI<\/jats:styled-content> square, Mann\u2013Whitney, Kaplan\u2013Mayer, and <jats:styled-content style=\"fixed-case\">ANOVA<\/jats:styled-content> tests. At the end of the study (12\u00a0weeks), the rate of complete response was 91.11% in the first group, and 84.66% and 78.33% in groups B and C, respectively (<jats:italic>P\u00a0<\/jats:italic>&lt;<jats:italic>\u00a0<\/jats:italic>0.05). The highest response rate was for the group treated with a standard dose of systemic <jats:styled-content style=\"fixed-case\">MA<\/jats:styled-content> and placebo. Our results showed that although oral cimetidine and low\u2010dose systemic <jats:styled-content style=\"fixed-case\">MA<\/jats:styled-content> had less efficacy in comparison to a standard dose of systemic <jats:styled-content style=\"fixed-case\">MA<\/jats:styled-content> in the treatment of <jats:styled-content style=\"fixed-case\">CL<\/jats:styled-content>, it still can be considered as a replacement therapy in high\u2010risk patients (such as patients with heart, kidney, and\/or liver disease) under close supervision of physicians.<\/jats:p>","DOI":"10.1111\/ijd.12709","type":"journal-article","created":{"date-parts":[[2015,6,24]],"date-time":"2015-06-24T23:03:36Z","timestamp":1435187016000},"page":"834-838","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":12,"title":["A comparative study between the efficacy of oral cimetidine and low\u2010dose systemic meglumine antimoniate (<scp>MA<\/scp>) with a standard dose of systemic <scp>MA<\/scp> in the treatment of cutaneous leishmaniasis"],"prefix":"10.1111","volume":"54","author":[{"given":"Siavash M.","family":"Shanehsaz","sequence":"first","affiliation":[{"name":"Department of Dermatology and Venereology Aleppo University Hospital Aleppo Syria"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Silva","family":"Ishkhanian","sequence":"additional","affiliation":[{"name":"Department of Dermatology and Venereology Aleppo University Hospital Aleppo Syria"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"311","published-online":{"date-parts":[[2015,6,24]]},"reference":[{"key":"e_1_2_6_2_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.cimid.2004.03.004"},{"key":"e_1_2_6_3_1","unstructured":"M Corrado 1892"},{"key":"e_1_2_6_4_1","first-page":"95","article-title":"Un nouveau zymogeme de Leishmania tropica, agent du Bouton d'Alep (Syrie)","volume":"56","author":"Belazzoug S","year":"1988","journal-title":"Arch Inst Pasteur Alger"},{"key":"e_1_2_6_5_1","doi-asserted-by":"publisher","DOI":"10.1016\/S0020-7519(02)00088-7"},{"key":"e_1_2_6_6_1","doi-asserted-by":"publisher","DOI":"10.1046\/j.1365-2230.2000.00664.x"},{"key":"e_1_2_6_7_1","doi-asserted-by":"publisher","DOI":"10.1016\/S0140-6736(98)10178-2"},{"key":"e_1_2_6_8_1","doi-asserted-by":"publisher","DOI":"10.1080\/00034983.1963.11686192"},{"key":"e_1_2_6_9_1","doi-asserted-by":"publisher","DOI":"10.1128\/AAC.27.6.916"},{"key":"e_1_2_6_10_1","first-page":"114","volume-title":"Cutaneous leishmaniasis","author":"Nilforoushzadeh MA","year":"2002"},{"key":"e_1_2_6_11_1","doi-asserted-by":"publisher","DOI":"10.1016\/S0923-1811(01)00147-5"},{"key":"e_1_2_6_12_1","doi-asserted-by":"publisher","DOI":"10.1097\/00000539-199907000-00040"},{"key":"e_1_2_6_13_1","doi-asserted-by":"publisher","DOI":"10.1046\/j.1365-2885.1999.00196.x"},{"key":"e_1_2_6_14_1","doi-asserted-by":"publisher","DOI":"10.1007\/s004030050331"},{"key":"e_1_2_6_15_1","first-page":"34","article-title":"Comparison of effects of Cimetidine and Glucantim in the treatment of cutaneous leishmaniasis in Balb\/c mice","volume":"4","author":"Izadi S","year":"2000","journal-title":"J\u00a0Shahrekord Uni Med Sci"},{"key":"e_1_2_6_16_1","doi-asserted-by":"crossref","first-page":"2603","DOI":"10.4049\/jimmunol.132.5.2603","article-title":"Monocyte suppression of antigen specific responses in diffuse cutaneous leishmaniasis patients, Dominican Republic","volume":"132","author":"Petersen EA","year":"1984","journal-title":"J Immunol"},{"key":"e_1_2_6_17_1","first-page":"185","volume-title":"Clinical Tropical Dermatology","author":"Conizares O","year":"1975"},{"key":"e_1_2_6_18_1","first-page":"807","article-title":"The control of leishmaniasis","volume":"58","author":"Marinkelle CJ","year":"1980","journal-title":"Bull World Health Organ"},{"key":"e_1_2_6_19_1","unstructured":"World Health Organization.The leishmaniasis. 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