We updated the design of this site on December 18, 2017. Learn more.
ClinicalTrials.gov
ClinicalTrials.gov Menu

The Association of Pelvic Organ Prolapse Severity and Urinary Symptoms/Sexual Function

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details.
ClinicalTrials.gov Identifier: NCT01436708
Recruitment Status : Recruiting
First Posted : September 20, 2011
Last Update Posted : September 7, 2016
Sponsor:
Information provided by (Responsible Party):

Study Description
Brief Summary:
Women with pelvic organ prolapse often accompany with urinary symptoms or sexual dysfunction, and analyzing the association will be helpful to identify the indication of proper management. Therefore, the aim of this study is to identify the above associations.

Condition or disease
Pelvic Organ Prolapse

Study Design

Study Type : Observational
Estimated Enrollment : 500 participants
Observational Model: Case-Only
Time Perspective: Prospective
Study Start Date : June 2011
Estimated Primary Completion Date : December 2017
Estimated Study Completion Date : June 2018

Resource links provided by the National Library of Medicine

U.S. FDA Resources

Groups and Cohorts


Outcome Measures

Eligibility Criteria

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Ages Eligible for Study:   20 Years to 99 Years   (Adult, Senior)
Sexes Eligible for Study:   Female
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population
all women with pelvic organ prolapse , especially with cystocele, in our outpatient department or the room of urodynamic studies.
Criteria

Inclusion Criteria:

  • all cases with with pelvic organ prolapse

Exclusion Criteria:

Contacts and Locations

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01436708


Locations
Taiwan
Far Eastern Memorial Hospital Recruiting
Banqiao, New Taipei, Taiwan, 220
Contact: Sheng-Mou Hsiao, M.D.    +886-2-89667000 ext 1424    smhsiao2@gmail.com   
Sponsors and Collaborators
Far Eastern Memorial Hospital
More Information

Responsible Party: Sheng-Mou Hsiao, Chief, Department of Obstetrics & Gynecology, Far Eastern Memorial Hospital
ClinicalTrials.gov Identifier: NCT01436708     History of Changes
Other Study ID Numbers: 100034-F
First Posted: September 20, 2011    Key Record Dates
Last Update Posted: September 7, 2016
Last Verified: September 2016

Keywords provided by Sheng-Mou Hsiao, Far Eastern Memorial Hospital:
pelvic organ prolapse
urinary symptoms
sexual function

Additional relevant MeSH terms:
Prolapse
Pelvic Organ Prolapse
Pathological Conditions, Anatomical