نمایش مختصر رکورد

dc.contributor.authorSahebari, Maryamen_US
dc.contributor.authorHeidari, Hosseinen_US
dc.contributor.authorNabavi, Shimaen_US
dc.contributor.authorKhodashahi, Mandanaen_US
dc.contributor.authorRezaieyazdi, Zahraen_US
dc.contributor.authorDadgarMoghaddam, Malihehen_US
dc.contributor.authorHosseinzadeh, Hosseinen_US
dc.contributor.authorAbbasi, Shaghayeghen_US
dc.contributor.authorHashemzadeh, Kamilaen_US
dc.date.accessioned1400-04-13T12:49:42Zfa_IR
dc.date.accessioned2021-07-04T12:49:42Z
dc.date.available1400-04-13T12:49:42Zfa_IR
dc.date.available2021-07-04T12:49:42Z
dc.date.issued2021-07-01en_US
dc.date.issued1400-04-10fa_IR
dc.date.submitted2019-12-14en_US
dc.date.submitted1398-09-23fa_IR
dc.identifier.citationSahebari, Maryam, Heidari, Hossein, Nabavi, Shima, Khodashahi, Mandana, Rezaieyazdi, Zahra, DadgarMoghaddam, Maliheh, Hosseinzadeh, Hossein, Abbasi, Shaghayegh, Hashemzadeh, Kamila. (2021). A double-blind placebo-controlled randomized trial of oral saffron in the treatment of rheumatoid arthritis. Avicenna Journal of Phytomedicine, 11(4), 332-342. doi: 10.22038/ajp.2020.17280en_US
dc.identifier.issn2228-7930
dc.identifier.issn2228-7949
dc.identifier.urihttps://dx.doi.org/10.22038/ajp.2020.17280
dc.identifier.urihttps://ajp.mums.ac.ir/article_17280.html
dc.identifier.urihttps://iranjournals.nlai.ir/handle/123456789/840436
dc.description.abstractObjective: Recently, saffron (Crocus sativus L. from the Iridaceae family) has been characterized by its antioxidant, anti-inflammatory and analgesic effects. This study aimed to evaluate the effect of saffron on disease activity in patients with rheumatoid arthritis (RA). Materials and Methods: This is a double-blind, placebo-controlled, randomized clinical trial (RCT) performed on 55 newly- diagnosed RA patients without previous treatment, who were randomly divided into intervention (included 28 cases) and control groups (consisted of 27 individuals). Standard therapy including prednisolone, oral methotrexate, folic acid, vitamin D, calcium, and alendronate, was administered similarly in both groups.  Patients received a 100 mg saffron pill/day (pure saffron powder) or placebo besides the standard protocol. The placebo had the same shape as the saffron pills. Follow up of DAS28ESR disease activity score was done on the 30th, 45th and 90th day of the study. Results: There was no difference between the intervention and control groups regarding to the DAS28ESR at the end of the study. However, a significant decrease in DAS28-ESR was observed in each group compared to the first visit (p=0.001). The results also showed no significant difference in the incidence of side effects in both groups. Conclusion: In summary, patients who received pure saffron pills (100 mg/day) in addition to standard therapy did not have a significant difference in improvement of disease activity from the patients on standard therapy.en_US
dc.languageEnglish
dc.language.isoen_US
dc.publisherMashhad University of Medical Sciencesen_US
dc.relation.ispartofAvicenna Journal of Phytomedicineen_US
dc.relation.isversionofhttps://dx.doi.org/10.22038/ajp.2020.17280
dc.subjectCrocus sativus Len_US
dc.subjectIridaceae familyen_US
dc.subjectSaffronen_US
dc.subjectRheumatoid arthritisen_US
dc.subjectClinical trialen_US
dc.subjectRCTen_US
dc.titleA double-blind placebo-controlled randomized trial of oral saffron in the treatment of rheumatoid arthritisen_US
dc.typeTexten_US
dc.typeOriginal Research Articleen_US
dc.contributor.departmentRheumatic Diseases Research Center, Mashhad University of Medical Sciences, Mashhad, Iranen_US
dc.contributor.departmentRheumatic Diseases Research Center, Mashhad University of Medical Sciences, Mashhad, Iranen_US
dc.contributor.departmentRheumatic Diseases Research Center, Mashhad University of Medical Sciences, Mashhad, Iranen_US
dc.contributor.departmentRheumatic Diseases Research Center, Mashhad University of Medical Sciences, Mashhad, Iranen_US
dc.contributor.departmentRheumatic Diseases Research Center, Mashhad University of Medical Sciences, Mashhad, Iranen_US
dc.contributor.departmentCommunity Medicine Department, faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iranen_US
dc.contributor.departmentDepartment of Pharmacodynamics and Toxicology, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iran. Pharmaceutical Research Center, Pharmaceutical Technology Institute, Mashhad University of Medical Sciences, Mashhad, Iranen_US
dc.contributor.departmentRheumatic Diseases Research Center, Mashhad University of Medical Sciences, Mashhad, Iranen_US
dc.contributor.departmentRheumatic Diseases Research Center, Mashhad University of Medical Sciences, Mashhad, Iranen_US
dc.citation.volume11
dc.citation.issue4
dc.citation.spage332
dc.citation.epage342
nlai.contributor.orcid0000-0002-2476-2478
nlai.contributor.orcid0000-0002-6689-0072
nlai.contributor.orcid0000-0002-0237-5485
nlai.contributor.orcid0000-0003-1198-1783
nlai.contributor.orcid0000-0001-8731-7999
nlai.contributor.orcid0000-0002-4797-8714
nlai.contributor.orcid0000-0002-8879-6263


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