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Endometrial and Myometrial Changes, With and Without Fibroids

This study has been withdrawn prior to enrollment.
(no enrollment)
Sponsor:
ClinicalTrials.gov Identifier:
NCT01671215
First Posted: August 23, 2012
Last Update Posted: April 15, 2015
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
Meir Medical Center
August 20, 2012
August 23, 2012
April 15, 2015
August 2012
August 2014   (Final data collection date for primary outcome measure)
ratio between normal & abnormal(by fibroid) uterine cavity [ Time Frame: year ]
Same as current
Complete list of historical versions of study NCT01671215 on ClinicalTrials.gov Archive Site
ratio between endometriom & myometrium area, circumference &n volume [ Time Frame: year ]
Same as current
Not Provided
Not Provided
 
Endometrial and Myometrial Changes, With and Without Fibroids
Endometrial and Myometrial Changes, With and Without Fibroids
fibroids are common among women in fertile age. the relation between fibroids and infertility is controversial. our goal is to claculate a ratio between uterine cavity - endometrium & myometrium in normal uterine s and study the interference of the cavity in uterine s with fibroids.

phase 1-

  1. retrospective measurments of uterine dimensions of 100 women with normal uterin
  2. measurment of the above during different sycle days in the same woman. 30 women.

phase 2- retrospective measurments of 500 uterine dimensions of women with fibroids phase 3- the same for 400 uterine malformations

Observational
Observational Model: Cohort
Time Perspective: Prospective
Not Provided
Not Provided
Probability Sample
women at the age of 20-45
Fibroids
Not Provided
Not Provided
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Withdrawn
0
Not Provided
August 2014   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  • women at IVF unit

Exclusion Criteria:

  • inabilty to measure propperly the uterine dimensions
Sexes Eligible for Study: Female
20 Years to 45 Years   (Adult)
Yes
Contact information is only displayed when the study is recruiting subjects
Israel
 
 
NCT01671215
MMC120026CTIL
No
Not Provided
Not Provided
Meir Medical Center
Meir Medical Center
Not Provided
Principal Investigator: ronni tepper, md Tel Aviv University
Meir Medical Center
April 2012