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Uphold Versus Robotic Surgery for Pelvic Prolapse Repair: A Decision Analytic Approach

Atlantic Health System logo

Atlantic Health System

Status

Completed

Conditions

Pelvic Organ Prolapse

Study type

Observational

Funder types

Other
Industry

Identifiers

NCT01611285
R10-04-002

Details and patient eligibility

About

Within the general objective of investigating optimal medical techniques for pelvic prolapse repair, this study proposes to: (1) test the hypothesis that the UPHOLD procedure is more cost effective than robotic surgery for pelvic prolapse repair (2)using formal decision analysis as the comparative strategy

Full description

The cumulative incidence of pelvic organ prolapse was approximately 2% in 2001. Given the aging demographics in the U.S., the incidence of prolapse is projected to increase to 30% or more for women aged 60 years and older and become of greater concern to both patients and physicians. The demand for gynecologic services is predicted to increase by more than 45% in the next ten years. Prolapse is related to childbirth, aging, defects in collagen, and smooth muscle structure and strength. Etiology includes intra-abdominal pressure from obesity, with obesity becoming an ever increasing factor in the US.

Treatment Choice of Patients:

Patients choose between pessary, surgery, and expectant management based on: age, prior prolapse surgery, preoperative pelvic pain scores, and pelvic organ prolapse severity. These are difficult decisions for patients.

When it comes to choosing between destinctive interventions with subtle advantages and disadvantages, patients typically want to hear their physician's views of the scientific merits of each procedure. Informed consent becomes extremely difficult when issues of cost-effectiveness are at hand. Thus, the proposed project.

Enrollment

20 patients

Sex

Female

Ages

18 to 90 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Female
  • Underwent either UPHOLD procedure or Robotic Surgery for Pelvic Organ prolapse

Exclusion criteria

  • Other vaginal procedure to correct prolapse

Trial design

20 participants in 2 patient groups

Robotic Sacrocolpopexy patients
Description:
Patients who underwent Robotic Sacrocolpopexy to treat pelvic organ prolapse between 2009 and 2010
UPHOLD patients
Description:
Patients who underwent the UPHOLD procedure to treat pelvic organ prolapse from 2009-2010.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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