Histomorphometry Analysis in Fertile and Infertile Patients

The recruitment status of this study is unknown because the information has not been verified recently.
Verified June 2012 by University of Sao Paulo.
Recruitment status was  Recruiting
Sponsor:
Information provided by (Responsible Party):
Dani Ejzenberg, MD, University of Sao Paulo
ClinicalTrials.gov Identifier:
NCT01623063
First received: June 15, 2012
Last updated: June 18, 2012
Last verified: June 2012

June 15, 2012
June 18, 2012
January 2012
June 2012   (final data collection date for primary outcome measure)
glandular volume [ Time Frame: 1 month ] [ Designated as safety issue: Yes ]
verify the glandular volume in fertile and infertil patients during the implantation window
Same as current
Complete list of historical versions of study NCT01623063 on ClinicalTrials.gov Archive Site
epitelial surface [ Time Frame: 1 month ] [ Designated as safety issue: Yes ]
to detect differences in the endometrium of fertile and infertile patients
Same as current
Not Provided
Not Provided
 
Histomorphometry Analysis in Fertile and Infertile Patients
Histomorphometry Analysis in Fertile and Infertile Patients

To detect similarities and differences in the endometrium of fertile and infertile patients

morphometric and pathologyc analysis of the endometrium in fertile and infertile patients

Interventional
Not Provided
Allocation: Non-Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Single Blind (Investigator)
Primary Purpose: Diagnostic
Infertility
Procedure: Hysteroscopy
hysteroscopy with guided biopsies
Other Names:
  • Bettocchi system- Karl Storz
  • pipelle- cornier
  • Experimental: Infertile
    patients from our human reproduction center
    Intervention: Procedure: Hysteroscopy
  • Active Comparator: Fertile
    patients with comproved fertility
    Intervention: Procedure: Hysteroscopy
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruiting
40
August 2012
June 2012   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • 18 to 41 years old
  • regular menses
  • infertility over 12 months

Exclusion Criteria:

  • previous uterine surgery
  • use of contraceptive pills or injections less than 3 months from the inclusion in the study
Female
18 Years to 41 Years
Yes
Contact: Dani Ejzenberg, MD 55 11 92828550 daejz@hotmail.com
Brazil
 
NCT01623063
EIFMUSP
No
Dani Ejzenberg, MD, University of Sao Paulo
University of Sao Paulo
Not Provided
Principal Investigator: Dani Ejzenberg University of Sao Paulo
University of Sao Paulo
June 2012

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP