Clinical Trials Logo

Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT01022372
Other study ID # 2009035
Secondary ID
Status Active, not recruiting
Phase N/A
First received November 30, 2009
Last updated May 9, 2011
Start date November 2009
Est. completion date December 2011

Study information

Verified date July 2010
Source Selcuk University
Contact n/a
Is FDA regulated No
Health authority Turkey: Ethics Committee
Study type Observational

Clinical Trial Summary

Our aim was to evaluate the efficacy of examining endometrial biopsy specimens for nerve fibers as a diagnostic test for endometriosis and endometrioma in a double-blind comparison with diagnostic laparoscopy.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 60
Est. completion date December 2011
Est. primary completion date June 2011
Accepts healthy volunteers No
Gender Female
Age group 17 Years to 45 Years
Eligibility Inclusion Criteria:

- Women in the reproductive age group undergoing laparoscopy for pelvic pain and/or infertility, and not currently receiving hormonal treatment for at least 3 months prior to laparoscopy will be included in the study

Study Design

Observational Model: Case Control, Time Perspective: Prospective


Related Conditions & MeSH terms

  • Endometriosis
  • Not Currently Receiving Hormonal Treatment for at Least 3 Months Prior to Laparoscopy.
  • Pelvic Pain
  • Undergoing Laparoscopy for Pelvic Pain and/or Infertility
  • Women in the Reproductive Age Group

Intervention

Procedure:
Endometrial biopsy
For all the groups

Locations

Country Name City State
Turkey The hospital of Meram medical Faculty Konya

Sponsors (1)

Lead Sponsor Collaborator
Selcuk University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary The density of nerve fibers in the endometrial biopsy sample. 1 year No