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Vitamin D During In Vitro Fertilisation (IVF) - A Prospective Randomized Trial

Phase 3
Conditions
Pregnancy Complication
Registration Number
NCT01019785
Lead Sponsor
Karolinska University Hospital
Brief Summary

During IVF treatment women will be randomized into supplementation with a high or a low dose of Vitamin D Main outcome Laboratory pregnancy, live pregnancy at 12 weeks, Baby take home rate, OHSS Secondary outcome: 1. Pregnancy complications (pregnancy hypertension, SGA, Diabetes) 2.Thrombin generation

Detailed Description

Not available

Recruitment & Eligibility

Status
UNKNOWN
Sex
Female
Target Recruitment
1000
Inclusion Criteria
  • All women initiating IVF treatment
Exclusion Criteria
  • Women that have entered the study before

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Laboratory pregnancy, live pregnancy at 12 weeks, take home baby rate4 weeks to 9 month
Secondary Outcome Measures
NameTimeMethod
Pregnancy complications (pregnancy hypertension, SGA, diabetes)9 months

Trial Locations

Locations (1)

IVF Unit Karolinska University Hospital, Huddinge

🇸🇪

Huddinge, Sweden

IVF Unit Karolinska University Hospital, Huddinge
🇸🇪Huddinge, Sweden

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