Do Patients With Early Post Operative Recurrence of Pelvic Organ Prolapse Have a Genetic Predisposition?

Sponsor
Atlantic Health System (Other)
Overall Status
Completed
CT.gov ID
NCT01614587
Collaborator
Reproductive Medicine Associates of New Jersey (Other)
50
1
37
1.4

Study Details

Study Description

Brief Summary

The objective is to explore the genetic predisposition to early pelvic organ prolapse after adequate surgical repair by exploring the association between pelvic organ prolapse recurrences and certain polymorphisms.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Pelvic organ prolapse develops as a result of a loss of support provided by the muscles and fascia that constitute the pelvic floor. Several recent population studies have estimated the prevalence of pelvic organ prolapse at between 10% and 30%. One in nine women will undergo surgery for these disorders in her lifetime and of these, one third will undergo repeated surgeries. The correction of pelvic organ protrusion is aimed at restoring the pelvic floor functional status and ultimately improving the patients quality of life. There are a few studies that have explored the genetic predisposition to developing pelvic organ prolapse but none so far looks at genetic factors involved in prolapse recurrence after adequate prolapse repair. There are two groups of women: women who underwent adequate repair of their prolapse and had an unexplained early recurrence. And a second control group of women who underwent the same prolapse repair procedure and had no further prolapse recurrence.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    50 participants
    Observational Model:
    Case-Control
    Time Perspective:
    Prospective
    Official Title:
    Do Patients With Early Post Operative Recurrence of Pelvic Organ Prolapse Have a Genetic Predisposition?
    Study Start Date :
    Mar 1, 2012
    Actual Primary Completion Date :
    Apr 1, 2015
    Actual Study Completion Date :
    Apr 1, 2015

    Arms and Interventions

    Arm Intervention/Treatment
    Cases

    Early, unexplained recurrence (within six months of procedure) after Sacrocolpopexy The recurrence required treatment (surgery or pessary)

    Controls

    Sacrocolpopexy during the same period No recurrence, no reoperation, no retreatment to date (minimum of 12 months from surgery)

    Outcome Measures

    Primary Outcome Measures

    1. SNP microarray analysis from recurrent prolapse subjects and controls [12 months post-operative, DNA will be collected]

      DNA will be evaluated by a variety of methods. For example, candidate polymorphisms may be evaluated using TaqMan SNP allelic discrimination assays which are based upon duplex real-time PCR. In addition, genome-wide SNP microarrays may be employed in order to perform a whole genome association study. Additional analysis such as DNA resequencing may also be required in order to identify causative polymorphisms linked to the newly associated SNPs. Other methods of DNA analysis such as next-generation sequencing may also be warranted.

    Secondary Outcome Measures

    1. Compare all peri-operative characteristics and demographics between groups [12 months post-operative]

      Perioperative data will include: age, date of surgery, repeat procedure or treatment, procedure and mesh used, mesh related complications, early post-operative complications. Descriptive statistics will be derived for the entire group. The two subgroups (case and control) will then be compared using: Student t test, Fisher exact test, and Wilcoxon rank-sum test for continuous, nonparametric categorical and nonparametric ordinal variables, respectively.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    N/A and Older
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Cases: early, unexplained recurrence (within 6 months of procedure) after sacrocolpopexy), the recurrence required treatment (surgery or pessary) Controls: sacrocolpopexy during the same period, no recurrence, no reoperation, no retreatment to date (minimum of 12 months from surgery)
    Exclusion Criteria:
    • Obvious surgical technical failure

    • Use of other graft material than polypropylene mesh

    • Planned two staged operation

    • Contraindications to surgery based on existing medical conditions

    • Pregnancy

    • Desire for pregnancy in the future

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Atlantic Health System Morristown New Jersey United States 07960

    Sponsors and Collaborators

    • Atlantic Health System
    • Reproductive Medicine Associates of New Jersey

    Investigators

    • Principal Investigator: Richard Scott, MD, Reproductive Medicine Associates
    • Principal Investigator: Patrick Culligan, MD, Atlantic Health System
    • Principal Investigator: Charbel Salamon, MD, Atlantic Health System

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Atlantic Health System
    ClinicalTrials.gov Identifier:
    NCT01614587
    Other Study ID Numbers:
    • R11-10-004
    First Posted:
    Jun 8, 2012
    Last Update Posted:
    Jun 9, 2017
    Last Verified:
    Jun 1, 2017

    Study Results

    No Results Posted as of Jun 9, 2017