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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00785993
Other study ID # 0703-C-017-AC
Secondary ID
Status Completed
Phase Phase 4
First received November 4, 2008
Last updated October 1, 2009
Start date November 2008
Est. completion date October 2009

Study information

Verified date October 2009
Source Instituto Valenciano de Infertilidad, IVI VALENCIA
Contact n/a
Is FDA regulated No
Health authority Spain: Ministry of Health
Study type Interventional

Clinical Trial Summary

Egg-banking would considerably simplify the logistics and means by which oocytes could be donated. These banks would make it easier to immediately provide oocytes that would be compatible to the recipient, shortening or even eliminating the problem of long waiting lists. Egg-banking would also allow the oocytes to be effectively quarantined, drastically diminishing the risk of transmission of infectious diseases in a fashion analogous to semen banks. The most essential prerequisite for a successful egg cryo-banking program is to have an efficient oocyte cryopreservation technology. Recent studies, including our own experience, have indicated that vitrified oocytes preserve intact their potential to fertilize and further develop into competent embryos, giving high clinical results as well as high survival rates. The aim of this study is to evaluate impact of the establishment of an egg-banking in our ovum donation program. Oocyte cryopreservation is carried out by Cryotop method. The study includes oocyte donation cycles conducted with fresh and vitrified oocytes. Recipients are allocated randomly into each group ("fresh vs. vitrified cycles"). Main outcome measures include survival, fertilization, embryo development and clinical outcome.


Recruitment information / eligibility

Status Completed
Enrollment 320
Est. completion date October 2009
Est. primary completion date September 2009
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 35 Years
Eligibility Inclusion Criteria:

- Receptors

- Women receiving donor oocytes and whose partners without seere pathology of semen.

- BMI < 25

Donors:

Inclusion Criteria:

18 - 35 years oldaƱos.

- Normal Response (8-15 follicles)to long protocol of ovarian stimulation with hCG

- Donors with normal menstrual cycles ( 21-35 day duration).

- Donors with Body Mass Index (BMI) between 18-25 Kg/m2

Exclusion Criteria:

- Donors with +/= two previous miscarriages`

- Polycystic Ovary Syndrome

- Donors with antecedents of poor embrionary quality not attributed to masculine factor.

- Donors with decline of Estradiol Hormone of more than 10% or Estradiol Hormone plateau.

- Donors with a high response >20 ovocitos and/or levels above 3000pg/mL of Estradiol the day of the administration of Chorionic gonadotropin (hCG.

Study Design

Allocation: Randomized, Endpoint Classification: Bio-equivalence Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Health Services Research


Related Conditions & MeSH terms


Intervention

Other:
Vitrification of oocytes for IVF treatment

Protocolary IVF treatment with fresh donor oocytes


Locations

Country Name City State
Spain Instituto Valenciano de Infertilidad Valencia

Sponsors (1)

Lead Sponsor Collaborator
Instituto Valenciano de Infertilidad, IVI VALENCIA

Country where clinical trial is conducted

Spain, 

Outcome

Type Measure Description Time frame Safety issue
Primary To evaluate the clinical outcome in an ovum donation program conducted with egg-banking. 14 days No