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OpenTrials
Completed

NCT Number: NCT00205023

Disseminated Endometrial Cancer Cells During Sonohysterography

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

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Key information

Age range

18 year and older

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

University of Wisconsin

Madison, Wisconsin, 53792, United States

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Stage I endometrial Cancer Disease
  • State IIA endometrial Cancer Disease

Exclusion criteria

  • Prior tubal ligation
  • Prior bilateral salpingectomy

Treatment and study plan

Sonohysterography

Procedure

SHG during surgery for endometrial cancer.

Primary outcomes

  1. determine the critical volume necessary to overcome tubal pressure and result in fluid dissemination during SHG

    Time frame: during surgery

Secondary outcomes

  1. evaluate the functional viability of any disseminated tumor cells collected during SHG

    Time frame: during surgery

Sponsors and collaborators

Lead sponsor

University of Wisconsin, Madison

Other

Registry information

Official study title

The Incidence of Disseminated Endometrial Cancer Cells During Sonohysterography and Their Functional Viability: a Prospective Study

Important dates

Study start
2004
Primary completion
2006
Study completion
2006
First posted
Sep 20, 2005
Registry last updated
Nov 19, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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