This trial is terminated!
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More info
You can access this
clinical trial
if you have
Fibroid Uterus or Quality of Life
and you are
between 21 and 45
years old
The phase for this study is not defined.
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The purpose

This study evaluates whether use of intraoperative ultrasound during laparoscopic or robotic myomectomy impacts quality of life. Half of participants will undergo laparoscopic or robotic myomectomy with use of the intraoperative ultrasound and half will undergo traditional laparoscopic or robotic myomectomy.

Provided treatments

  • Procedure: Intraoperative contact ultrasonography

Locations near you

Unfortunately, there are no recruiting locations near you. Please check the list with all locations below.
Tris trial is registered with FDA with number: NCT02879058. The sponsor of the trial is The Cleveland Clinic and it is looking for 140 volunteers for the current phase.
Official trial title:
The Effect of Intraoperative Contact Sonography on Quality of Life Following Laparoscopic or Robotic Myomectomy