<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>2013</volume><submitter>Carbonell JL</submitter><pubmed_abstract>Objectives. To evaluate the efficacy, safety, and quality of life by using 2.5 and mifepristone 5 mg daily doses to treat uterine fibroids over 3 months with a 9-month followup period. Design. Randomized clinical trial. Place. "Eusebio Hernández" Hospital, Havana, Cuba. Subjects. 220 women with symptomatic uterine fibroids. Treatment. One-half (2.5 mg) or one-whole 5 mg mifepristone tablet. Variables to Evaluate Efficacy. Changes in fibroid and uterine volumes, in symptomatic prevalence and intensity, and in quality of life. Results. After 3-month treatment, fibroid volume decreased by 27.9% (CI 95% 20-35) and 45.5% (CI 95% 37-62), in the 2.5 and 5 mg groups, respectively, P = 0.003. There was no difference in the prevalence of symptoms at the end of treatment, unlike after 6- and 9-month </pubmed_abstract><journal>ISRN obstetrics and gynecology</journal><pagination>649030</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3747426</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Treatment of Uterine Myoma with 2.5 or 5 mg Mifepristone Daily during 3 Months with 9 Months Posttreatment Followup: Randomized Clinical Trial.</pubmed_title><pmcid>PMC3747426</pmcid><pubmed_authors>Garces R</pubmed_authors><pubmed_authors>Carbonell JL</pubmed_authors><pubmed_authors>Sanchez C</pubmed_authors><pubmed_authors>Perez Y</pubmed_authors><pubmed_authors>Acosta R</pubmed_authors><pubmed_authors>Tomasi G</pubmed_authors></additional><is_claimable>false</is_claimable><name>Treatment of Uterine Myoma with 2.5 or 5 mg Mifepristone Daily during 3 Months with 9 Months Posttreatment Followup: Randomized Clinical Trial.</name><description>Objectives. To evaluate the efficacy, safety, and quality of life by using 2.5 and mifepristone 5 mg daily doses to treat uterine fibroids over 3 months with a 9-month followup period. Design. Randomized clinical trial. Place. "Eusebio Hernández" Hospital, Havana, Cuba. Subjects. 220 women with symptomatic uterine fibroids. Treatment. One-half (2.5 mg) or one-whole 5 mg mifepristone tablet. Variables to Evaluate Efficacy. Changes in fibroid and uterine volumes, in symptomatic prevalence and intensity, and in quality of life. Results. After 3-month treatment, fibroid volume decreased by 27.9% (CI 95% 20-35) and 45.5% (CI 95% 37-62), in the 2.5 and 5 mg groups, respectively, P = 0.003. There was no difference in the prevalence of symptoms at the end of treatment, unlike after 6- and 9-month </description><dates><release>2013-01-01T00:00:00Z</release><publication>2013</publication><modification>2025-05-29T21:07:22.575Z</modification><creation>2025-05-29T21:07:22.575Z</creation></dates><accession>S-EPMC3747426</accession><cross_references><pubmed>23984082</pubmed><doi>10.1155/2013/649030</doi></cross_references></HashMap>