<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>7(1)</volume><submitter>Harada T</submitter><pubmed_abstract>&lt;h4>Objective&lt;/h4>To study the impact of estetrol (E4), a novel native estrogen with selective tissue activity, on endometriosis-associated pelvic pain (EAPP) and global impressions of endometriosis pain.&lt;h4>Design&lt;/h4>Multicenter, randomized, open-label, active-controlled study; 88 eligible Japanese participants with endometriosis were randomized to either the E4 15 mg/drospirenone (DRSP) 3 mg group or the ethinyl estradiol (EE) 20 μg/DRSP 3 mg group. Participants received assigned treatment for 12 weeks.&lt;h4>Subjects&lt;/h4>Japanese patients aged ≥20 and &lt;50 years diagnosed with endometriosis. Eligibility required an EAPP score ≥40 mm on the visual analogue scale (VAS).&lt;h4>Intervention&lt;/h4>Participants were randomized 1:1 to E4/DRSP or EE/DRSP groups.&lt;h4>Main outcome measures&lt;/h4>Change in E</pubmed_abstract><journal>F&amp;S reports</journal><pagination>38-45</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12905615</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Impact of estetrol and drospirenone combination therapy on alleviation of the pelvic pain of endometriosis: a randomized control trial.</pubmed_title><pmcid>PMC12905615</pmcid><pubmed_authors>Harada T</pubmed_authors><pubmed_authors>Meguro K</pubmed_authors><pubmed_authors>Kobayashi T</pubmed_authors><pubmed_authors>Nogami M</pubmed_authors><pubmed_authors>Iizuka M</pubmed_authors><pubmed_authors>Manda C</pubmed_authors><pubmed_authors>Hirayama M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Impact of estetrol and drospirenone combination therapy on alleviation of the pelvic pain of endometriosis: a randomized control trial.</name><description>&lt;h4>Objective&lt;/h4>To study the impact of estetrol (E4), a novel native estrogen with selective tissue activity, on endometriosis-associated pelvic pain (EAPP) and global impressions of endometriosis pain.&lt;h4>Design&lt;/h4>Multicenter, randomized, open-label, active-controlled study; 88 eligible Japanese participants with endometriosis were randomized to either the E4 15 mg/drospirenone (DRSP) 3 mg group or the ethinyl estradiol (EE) 20 μg/DRSP 3 mg group. Participants received assigned treatment for 12 weeks.&lt;h4>Subjects&lt;/h4>Japanese patients aged ≥20 and &lt;50 years diagnosed with endometriosis. Eligibility required an EAPP score ≥40 mm on the visual analogue scale (VAS).&lt;h4>Intervention&lt;/h4>Participants were randomized 1:1 to E4/DRSP or EE/DRSP groups.&lt;h4>Main outcome measures&lt;/h4>Change in E</description><dates><release>2026-01-01T00:00:00Z</release><publication>2026 Feb</publication><modification>2026-07-15T16:35:38.367Z</modification><creation>2026-07-07T03:08:39.476Z</creation></dates><accession>S-EPMC12905615</accession><cross_references><pubmed>41694262</pubmed><doi>10.1016/j.xfre.2025.12.002</doi></cross_references></HashMap>