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ovel approaches in IVF.

Completed
Registration Number
NL-OMON23935
Lead Sponsor
Department of Reproductive Medicine, University Medical Center, Utrecht, The Netherlands.
Brief Summary

1. Lancet. 2007 Mar 3;369(9563):743-9.<br> <br><br> 2. Hum Reprod. 2008 Feb;23(2):316-23. Epub 2007 Nov 22.<br> <br><br> 3. Ned Tijdschr Geneeskd. 2008 Apr 5;152(14):809-16.

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
400
Inclusion Criteria

Patients with an indication for IVF or IVF/ Intracytoplasmic Sperm Injection (ICSI) based on tubal, male or unexplained infertility were recruited. Patients under < 38 years with a normal menstrual cycle (cycle length between period 25-35 days) and without severe obesity or underweight (body mass index (BMI) 18-28 kg/m2) were eligible for the study.

Exclusion Criteria

N/A

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The primary outcome parameters chosen for this study were: <br /><br>1. Pregnancy within one year of treatment after randomization leading to term (¡Ý 37 weeks gestation) live birth;<br /><br>2. Total costs per couple and child up to 6 weeks after expected delivery, and (3) patient discomfort/distress during IVF treatment. <br />
Secondary Outcome Measures
NameTimeMethod
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