Do Patients With Early Post Operative Recurrence of Pelvic Organ Prolapse Have a Genetic Predisposition?
- Full Text View
- Tabular View
- No Study Results Posted
- Disclaimer
- How to Read a Study Record
Purpose
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 |
|---|
|
Pelvic Organ Prolapse |
| Study Type: | Observational |
| Study Design: | Observational Model: Case Control Time Perspective: Prospective |
| Official Title: | Do Patients With Early Post Operative Recurrence of Pelvic Organ Prolapse Have a Genetic Predisposition? |
- SNP microarray analysis from recurrent prolapse subjects and controls [ Time Frame: 12 months post-operative, DNA will be collected ] [ Designated as safety issue: No ]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 indentify causative polymorphisms linked to the newly associated SNPs. Other methods of DNA analysis such as next-generation sequencing may also be warranted.
- Compare all peri-operative characteristics and demographics between groups [ Time Frame: 12 months post-operative ] [ Designated as safety issue: No ]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.
Biospecimen Retention: Samples With DNA
DNA obtained from a buccal swab
| Estimated Enrollment: | 60 |
| Study Start Date: | March 2012 |
| Estimated Study Completion Date: | June 2013 |
| Estimated Primary Completion Date: | December 2012 (Final data collection date for primary outcome measure) |
| Groups/Cohorts |
|---|
Cases
|
Controls
|
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.
Eligibility| Genders Eligible for Study: | Female |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Probability Sample |
Women suffering from pelvic organ prolapse
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| Contact: Patrick Culligan, MD | 973-971-7267 | |
| Contact: Richard Scott, MD |
| United States, New Jersey | |
| Atlantic Health System | Recruiting |
| Morristown, New Jersey, United States, 07960 | |
| Contact: Jodie Komar, BSN 973-971-7426 | |
| Principal Investigator: Patrick Culligan, MD | |
| Sub-Investigator: Charbel Salamon, MD | |
| Principal Investigator: Richard Scott, MD | |
| Principal Investigator: | Richard Scott, MD | Reproductive Medicine Associates |
| Principal Investigator: | Patrick Culligan, MD | Atlantic Health System |
| Principal Investigator: | Charbel Salamon, MD | Atlantic Health System |
More Information
No publications provided
| Responsible Party: | Jodie Komar, Charbel Salamon, MD. Director, Gynecologic Robotic Surgery, Atlantic Health System |
| ClinicalTrials.gov Identifier: | NCT01614587 History of Changes |
| Other Study ID Numbers: | R11-10-004 |
| Study First Received: | May 31, 2012 |
| Last Updated: | June 7, 2012 |
| Health Authority: | United States: Institutional Review Board |
Keywords provided by Atlantic Health System:
|
pelvic organ prolapse recurrence of pelvic organ prolapse pelvic floor genetic predisposition SNP microarray analysis genetic factors adequate prolapse repair polymorphisms |
surgical failure reoperation DNA buccal swabs TaqMan SNP allelic discrminiation assays duplex real-time PCR genome-wide SNP microarrays next-generation sequencing |
Additional relevant MeSH terms:
|
Disease Susceptibility Genetic Predisposition to Disease Prolapse Recurrence |
Pelvic Organ Prolapse Disease Attributes Pathologic Processes Pathological Conditions, Anatomical |
ClinicalTrials.gov processed this record on May 19, 2013