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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

πŸ‡ΈπŸ‡ͺ

Huddinge, Sweden

IVF Unit Karolinska University Hospital, Huddinge
πŸ‡ΈπŸ‡ͺHuddinge, Sweden

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