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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00205023
Other study ID # CO03702
Secondary ID H-2003-0499A5328
Status Completed
Phase N/A
First received
Last updated
Start date January 2004
Est. completion date August 2006

Study information

Verified date June 2008
Source University of Wisconsin, Madison
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of study is to: 1) determine critical volume necessary to overcome tubal pressure and result in fluid dissemination and 2) evaluate functional viability of any disseminated tumor cells collected during SHG


Recruitment information / eligibility

Status Completed
Enrollment 25
Est. completion date August 2006
Est. primary completion date February 2006
Accepts healthy volunteers No
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Stage I endometrial Cancer Disease

- State IIA endometrial Cancer Disease

Exclusion Criteria:

- Prior tubal ligation

- Prior bilateral salpingectomy

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Sonohysterography
SHG during surgery for endometrial cancer.

Locations

Country Name City State
United States University of Wisconsin Madison Wisconsin

Sponsors (1)

Lead Sponsor Collaborator
University of Wisconsin, Madison

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary determine the critical volume necessary to overcome tubal pressure and result in fluid dissemination during SHG during surgery
Secondary evaluate the functional viability of any disseminated tumor cells collected during SHG during surgery
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