Restorelle® Mesh Versus Native Tissue Repair for Prolapse

Trial ID or NCT#

NCT02162615

Status

recruiting iconRECRUITING

Purpose

The purpose of this study is to collect information on the safety and effectiveness of Restorelle Direct Fix mesh and the surgical procedure to implant Restorelle. These results will be compared to the safety and effectiveness results in patients who have native tissue repair (without mesh) as their pelvic organ prolapse treatment.

Official Title

Restorelle® Transvaginal Mesh Versus Native Tissue Repair for Treatment of Pelvic Organ Prolapse, Restorelle 522 Study

Eligibility Criteria

Ages Eligible for Study: Older than 18 Years
Sexes Eligible for Study: Female
Accepts Healthy Volunteers: No
Inclusion Criteria:
  1. - Female at least 18 years of age - Subject has pelvic organ prolapse with leading edge at or beyond the hymen. At or beyond the hymen is defined as POP-Q scores of Ba ≥0 and C≥ -1/2 tvl or Bp ≥0 and C≥ -1/2 tvl - Subject reports a bothersome bulge they can see or feel per PFDI-20 question 3, response of 2 or higher (i.e. responses of "somewhat", "moderately" or "quite a bit") - Subject is willing to provide written informed consent - Subject is willing and able to comply with the follow-up regimen
Exclusion Criteria:
  1. - Subject is pregnant or intends to become pregnant during the study - Subject has an active or chronic systemic infection including any gynecologic infection, untreated urinary tract infection (UTI), or tissue necrosis - Subject has a history of pelvic organ cancer (e.g. uterine, ovarian, bladder, or cervical) - Subject has had prior or is currently undergoing radiation, laser therapy, or chemotherapy in the pelvic area - Subject has taken systemic steroids (within the last month), or immunosuppressive or immunomodulatory treatment (within the last 3 months) - Subject has a systemic connective tissue disease (e.g. scleroderma, systemic lupus erythematosus (SLE), Marfan syndrome, Ehlers Danlos, collagenosis, polymyositis or polymyalgia rheumatica) - Subject has chronic systemic pain that includes the pelvic area or chronic focal pain that involves the pelvis - Subject has uncontrolled diabetes mellitus (DM) - Subject has a known neurologic or medical condition affecting bladder function (e.g. multiple sclerosis, spinal cord injury, or stroke with residual neurologic deficit) - Subject is seeking obliterative vaginal surgery as treatment for pelvic organ prolapse (colpocleisis) - Subject is not able to conform to the modified dorsal lithotomy position - Subject is currently participating in or plans to participate in another device or drug study during this study - Subject has a known sensitivity to polypropylene - Subject has had previous prolapse repair with mesh in the target compartment(s) - Subject is planning to undergo a concomitant prolapse repair in a non-target compartment with anything other than native tissue repair
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Investigator(s)

Eric R. Sokol, MD
Eric R. Sokol, MD
Urogynecologist, Pelvic surgeon, Minimally invasive gynecologic surgeon, Pelvic reconstructive surgeon, Obstetrician and Gynecologist (OB-GYN)
Associate Professor of Obstetrics and Gynecology (Gynecology-Urogynecology) and, by courtesy, of Urology

View on ClinicalTrials.gov