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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01980563
Other study ID # EC/2010/367
Secondary ID
Status Completed
Phase N/A
First received October 24, 2013
Last updated November 4, 2013
Start date January 2011
Est. completion date December 2012

Study information

Verified date November 2013
Source University Hospital, Ghent
Contact n/a
Is FDA regulated No
Health authority Belgium: Ethics Committee
Study type Interventional

Clinical Trial Summary

Monitoring ovarian stimulation for in vitro fertilization (IVF) and intracytoplasmatic sperm injection (ICSI) can be simplified by reducing the procedure to measuring follicles by ultrasound. Proponents of a simplified procedure claim that the procedure can be reduced to simple monitoring by ultrasound while maintaining results (numbers of mature oocytes, percentage of pregnancy and live birth rates). On the other hand simultaneous blood sampling for measuring hormone levels is still the state of the art in many clinics. A large review (Cochrane review) stated that "although there was no clear evidence for a better outcome, combined cycle monitoring was still recommended until it could be proven that ovarian hyperstimulation can be avoided without hormonal monitoring". Investigators therefore perform a study that compares the results between 2 groups: those with ultrasound monitoring and those with combined monitoring. Deciding when to plan the retrieval of the oocytes can depend on subtle differences in the number of large follicles measured by ultrasound, but also on hormonal levels in the blood of the patient. Therefore the investigators planned a randomized study in the group of patients with combined monitoring. The investigators examined if delaying the moment for planning the moment of oocyte retrieval by 24 hours had any effect on the number of mature oocytes and pregnancy rates and what the effect of rising progesterone levels might be. The investigators hypothesis was that combined monitoring could lead to better results since recent studies have thought that rising progesterone levels, if found, have a negative impact on pregnancy rates. On the other hand the investigators expect to find that waiting for larger follicles in cases with normal progesterone levels lead to a better oocyte yield.


Recruitment information / eligibility

Status Completed
Enrollment 416
Est. completion date December 2012
Est. primary completion date December 2011
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 45 Years
Eligibility inclusion criteria:

- absence of ovarian cysts

- both ovaries present

exclusion criteria:

- ovarian cysts

- not both ovaries present

Study Design

Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms

  • Efficiency in Terms of Mature Oocyte Yield

Intervention

Procedure:
ultrasound

combined monitoring


Locations

Country Name City State
Belgium University Hospital Ghent

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Ghent

Country where clinical trial is conducted

Belgium, 

Outcome

Type Measure Description Time frame Safety issue
Primary The number of mature oocytes obtained. 1 day No
Secondary The number of fertilized oocytes/good quality embryos at the moment of egg retrieval up to embryo transfer, assessed up to 100 months No
Secondary Pregnancy rate 12 months after egg retrieval No
Secondary clinical pregnancy rate 12 months after egg retrieval No
Secondary ongoing pregnancy rate 12 months after egg retrieval No
Secondary live birth rate for each individual transferred embryo 12 months after egg retrieval No