{"id":3263,"date":"2021-09-29T14:34:04","date_gmt":"2021-09-29T12:34:04","guid":{"rendered":"https:\/\/profertil-female.eu\/?page_id=3263"},"modified":"2025-01-20T09:49:29","modified_gmt":"2025-01-20T08:49:29","slug":"ivf-studie","status":"publish","type":"page","link":"https:\/\/profertil-female.eu\/at\/studien\/ivf-studie\/","title":{"rendered":"AKH-Studie"},"content":{"rendered":"\n
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\u00dcberlegener synergistischer
Effekt<\/h1>\n<\/div><\/div>\n\n\n\n
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Verbesserung<\/mark> der Fertilisationsrate, Embryoqualit\u00e4t und Schwangerschaftsrate<\/h2>\n<\/div>\n\n\n\n
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AKH-STUDIE 2017<\/p>\n\n\n\n

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Anzahl der Patienten:
<\/strong>n = 100<\/p>\n\n\n\n

(PROFERTIL\u00ae female Gruppe
n = 50; Kontrollgruppe n = 50)<\/p>\n<\/div>\n<\/div>\n\n\n\n

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Studiendesign<\/strong>
Pilotstudie \u2013 offene, prospektive, randomisierte, klinische Fall-Kontroll-Studie
Anzahl Patientinnen: 100<\/p>\n\n\n\n

Klinische Studie zur Beforschung der Formulierung von PROFERTIL\u00ae female
<\/strong>The Impact of a Standardized Oral Multinutrient Supplementation on Embryo Quality in in vitro Fertilization\/Intracytoplasmic Sperm Injection: A Prospective Randomized Trial<\/p>\n\n\n\n

Studienziele<\/strong>
Prim\u00e4res Ziel dieser Pilotstudie war es, den Behandlungseffekt von PROFERTIL\u00ae female (im Vergleich zu 400 mcg Fols\u00e4ure) auf die Embryonenqualit\u00e4t von Frauen im Rahmen einer IVF-Behandlung zu bestimmen. Als sekund\u00e4res Ziel der Studie wurde die klinische Schwangerschaftsrate ausgewertet.<\/p>\n\n\n\n

Ergebnisparameter<\/strong><\/p>\n\n\n\n

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  1. Embryonenqualit\u00e4t am 3. Tag nach der Entnahme der Oozyten (gute Qualit\u00e4t vs. schlechte Qualit\u00e4t)<\/li>\n\n\n\n
  2. Klinische Schwangerschaftsrate<\/li>\n<\/ol>\n\n\n\n
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    *Nouri K. et al., Gynecol Obstet Invest. 2017;82(1):8-14.<\/a><\/em><\/p>\n<\/div>\n\n\n\n

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    <\/div>\n<\/div><\/div>\n","protected":false},"excerpt":{"rendered":"

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