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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00848185
Other study ID # IVIMAD-MC-10-2008-01
Secondary ID
Status Completed
Phase
First received
Last updated
Start date June 2008
Est. completion date March 2009

Study information

Verified date April 2018
Source IVI Madrid
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Introduction OHSS still remains a complication of assisted reproduction treatments. hCG administration to trigger final oocyte maturation will release vascular mediators, being VEGF and other proteins such as VE-Cadherin or Angiopoietin- 2. It has been shown that replacing hCG by GnRH agonists will induce a very short endogenous LH peak, potent enough to induce final oocyte maturation but no OHSS will develop. The investigators examined VEGF, VE-Cadherin and Angiopoietin-2 modulation by hCG as well as GnRH agonists in oocyte donors undergoing controlled ovarian stimulation.


Description:

Material and Methods Between June and December of 2008 we evaluated 90 egg donors. They underwent COH with 150 IU rFSH as starting dose, we separated them in 3 groups (n:30 each): Groups 1 and 2 received a 0.25mg daily dose of GnRH antagonist when a follicle 14mm in diameter was observed. hCG 250g was given to group 1 while group 2 received triptorelin 0.2mg when leading two follicles were 17mm. Group 3 was stimulated with standard long protocol, hCG was given following similar criteria.

Blood was collected the day of hCG/aGnRH administration as well as the day of egg retrieval, and follicular fluid from the first two mature follicles was also frozen. We collected granulosa cells (GC) of 10 patients of each group as well Levels of VEGF, sVE-Cadherin an Angiopietin 2 were determined by ELISA in serum and in follicular fluid.

Results were analyzed via ANOVA.Data are expressed as meanĀ± SEM. A significant difference was defined as p< 0.05.


Recruitment information / eligibility

Status Completed
Enrollment 96
Est. completion date March 2009
Est. primary completion date February 2009
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 34 Years
Eligibility Inclusion Criteria:

- Donors

Exclusion Criteria:

- Important diseases

Study Design


Related Conditions & MeSH terms

  • Vascular Endothelial Growth Factor Overexpression

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
IVI Madrid

Outcome

Type Measure Description Time frame Safety issue
Primary VEGF Protein and mRNA Levels VEGF concentration in follicular fluid and VEGF mRNA expression in granulosa cells from patients who received either GnRH agonist instead of hCG 1 year
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