Robotic Assisted Sacral Colpopexy : A Prospective Study Assessing Outcomes With Learning Curves

Status unconfirmed · Not applicable

Conditions studied: Pelvic Organ Prolapse

In brief

The investigators scientific aims are to determine the benefits associated with the use of robotic assisted laparoscopic sacrocolpopexy surgery on women with prolapse, to define how the benefits impact the patient, physician and the institution, and to determine the complications associated with the use of the robot. This will be a prospective cohort following 100 patients for a 24 month period.

Key facts

Study ID

NCT01535833

Run by

Kaiser Permanente

People needed

100

Starts

2012-02-01

Expected to finish

2016-12-01

Last updated by the study team

2016-05-12

Who can join

Age: 18 and older, up to 80. Sex: female. Healthy volunteers: accepted.

You may qualify if…

• > 18 years old
• Females only
• Undergoing robotic assisted laparoscopic sacrocolpopexy with or without other procedures for pelvic organ prolapse
• Willing to return for follow-up visits
• Written informed consent obtained from each subject

You may not qualify if…

• Decline to participate
• Pregnant or contemplating future pregnancy (within a year)
• Unable to participate in the informed consent process

Where it is running

• Kaiser Permanente San Diego — San Diego, California, United States (enrolling)
• Kaiser Permanente Downey — Los Angeles, California, United States

Full record on ClinicalTrials.gov

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