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Clinical Trials/NCT01842178
NCT01842178
Withdrawn
Not Applicable

Randomized Prospective Study of Endometrial Injury in In Vitro Fertilization Cycles With Oocyte Donation

Centro de Infertilidad y Reproducción Humana1 site in 1 countryApril 2013
ConditionsSubfertility

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Subfertility
Sponsor
Centro de Infertilidad y Reproducción Humana
Locations
1
Primary Endpoint
biochemical pregnancy
Status
Withdrawn
Last Updated
8 years ago

Overview

Brief Summary

This study is designed to evaluate the potential benefit in pregnancy rates produced by an endometrial scratching made in an IVF cycle prior to embryo transfer in patients with donated oocytes.

Detailed Description

This is a randomized, comparative, prospective, double Blind study. The First stage of this study consists of revising the patients medical records to identify possible candidates. Patients indicated are randomized into two groups: experimental and control. They are followed up to 12 week of pregnancy.

Registry
clinicaltrials.gov
Start Date
April 2013
End Date
January 2017
Last Updated
8 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Sponsor
Centro de Infertilidad y Reproducción Humana
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Do IVF cycle with donor eggs
  • Will adjust to protocol for the study.
  • Have signed informed consent

Exclusion Criteria

  • Clinically significant systemic disease, hypothalamic or pituitary tumors
  • ovarian, uterine or breast cancer
  • hormonal abnormalities and / or medical , biochemistry, hematology pathology, which might interfere with gonadotropin treatment.
  • known positivity for human immunodeficiency virus (HIV), hepatitis C or B virus (HCV / HBV) of the candidate or her partner.
  • Uterine Factor(submucosal fibroids, intramural fibroids\> 4 cm)
  • Hydrosalpinx
  • Patients receiving immune treatment
  • Positive Diagnosis Thrombophilia
  • preimplantation genetic diagnosis needed
  • In case of using marital sperm are excluded the following patients:Altered male karyotype, Altered Meiosis in testicular biopsy, Altered FISH, sperm Fragmentation\> 45%

Outcomes

Primary Outcomes

biochemical pregnancy

Time Frame: 14-16 days post-follicular punction

Determination of human chorionic gonadotropin blood levels.

Secondary Outcomes

  • Clinical pregnancy(6 pregnancy weeks)

Study Sites (1)

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