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Women with\n                      <jats:styled-content style=\"fixed-case\">PCOS<\/jats:styled-content>\n                      , diagnosed according to the modified 2003 Rotterdam criteria, received three cycles of either\n                      <jats:styled-content style=\"fixed-case\">E4<\/jats:styled-content>\n                      15\u2009mg\/\n                      <jats:styled-content style=\"fixed-case\">DRSP<\/jats:styled-content>\n                      3\u2009mg or\n                      <jats:styled-content style=\"fixed-case\">EE<\/jats:styled-content>\n                      30\u2009mcg\/\n                      <jats:styled-content style=\"fixed-case\">DRSP<\/jats:styled-content>\n                      3\u2009mg. After a 2\u2010month washout, participants crossed over to the alternate regimen for three further cycles. Glucose tolerance (via 75\u2009g oral glucose tolerance test [\n                      <jats:styled-content style=\"fixed-case\">OGTT<\/jats:styled-content>\n                      ]), insulin levels and homeostatic model assessment for insulin resistance (\n                      <jats:styled-content style=\"fixed-case\">HOMA<\/jats:styled-content>\n                      \u2010\n                      <jats:styled-content style=\"fixed-case\">IR<\/jats:styled-content>\n                      ) were compared between treatments.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      Of 66 women enrolled, 61 completed both treatment phases. Baseline characteristics were comparable. No significant differences were observed in the mean changes in 2\u2010h\n                      <jats:styled-content style=\"fixed-case\">OGTT<\/jats:styled-content>\n                      (\n                      <jats:styled-content style=\"fixed-case\">E4<\/jats:styled-content>\n                      \/\n                      <jats:styled-content style=\"fixed-case\">DRSP<\/jats:styled-content>\n                      : 4.65\u2009mg\/\n                      <jats:styled-content style=\"fixed-case\">dL<\/jats:styled-content>\n                      [95% confidence interval (\n                      <jats:styled-content style=\"fixed-case\">CI<\/jats:styled-content>\n                      ) \u22122.37 to 11.66] vs.\n                      <jats:styled-content style=\"fixed-case\">EE<\/jats:styled-content>\n                      \/\n                      <jats:styled-content style=\"fixed-case\">DRSP<\/jats:styled-content>\n                      : 14.40\u2009mg\/\n                      <jats:styled-content style=\"fixed-case\">dL<\/jats:styled-content>\n                      [95%\n                      <jats:styled-content style=\"fixed-case\">CI<\/jats:styled-content>\n                      7.50\u201321.29];\n                      <jats:italic>p<\/jats:italic>\n                      \u2009=\u20090.05; upper boundary for non\u2010inferiority margin of 14.29), 1\u2010h insulin levels (\u22121.04\u2009\n                      <jats:styled-content style=\"fixed-case\">\u03bcU<\/jats:styled-content>\n                      \/\n                      <jats:styled-content style=\"fixed-case\">mL<\/jats:styled-content>\n                      [95%\n                      <jats:styled-content style=\"fixed-case\">CI<\/jats:styled-content>\n                      \u221225.94 to 23.86] vs. \u22120.77\u2009\n                      <jats:styled-content style=\"fixed-case\">\u03bcU<\/jats:styled-content>\n                      \/\n                      <jats:styled-content style=\"fixed-case\">mL<\/jats:styled-content>\n                      [95%\n                      <jats:styled-content style=\"fixed-case\">CI<\/jats:styled-content>\n                      \u221225.24 to 23.70];\n                      <jats:italic>p<\/jats:italic>\n                      \u2009=\u20090.99; upper boundary for non\u2010inferiority margin of 50.72) or\n                      <jats:styled-content style=\"fixed-case\">HOMA<\/jats:styled-content>\n                      \u2010\n                      <jats:styled-content style=\"fixed-case\">IR<\/jats:styled-content>\n                      (0.28 [95%\n                      <jats:styled-content style=\"fixed-case\">CI<\/jats:styled-content>\n                      \u22120.24 to 0.80] vs. 0.60 [95%\n                      <jats:styled-content style=\"fixed-case\">CI<\/jats:styled-content>\n                      0.09\u20131.11];\n                      <jats:italic>p<\/jats:italic>\n                      \u2009=\u20090.39; upper boundary for non\u2010inferiority margin of 1.06).\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusion<\/jats:title>\n                    <jats:p>E4\/DRSP was not inferior to EE\/DRSP in its effects on glucose tolerance, insulin levels and HOMA\u2010IR, supporting its use as a potential oral contraceptive option in women with PCOS.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.1111\/dom.70126","type":"journal-article","created":{"date-parts":[[2025,9,12]],"date-time":"2025-09-12T08:51:22Z","timestamp":1757667082000},"page":"7244-7257","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":3,"title":["Effects of estetrol\/drospirenone versus ethinyl estradiol\/drospirenone on glucose tolerance in women with polycystic ovary syndrome: A randomised controlled 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