NCT00729417

Brief Summary

Evaluation of Obstetrical Risk Factors for the development of Urinary and/or Fecal Incontinence according to a questionaire The questionaire will be filled by the study investigators after the women participating in the study sign their consent. The study is based solely on a questionaire and does not include any physical examination, blood exam or intervention. The study will be performed on the premises of Maaynei Hayeshua medical center. The inclusion criteria include women above the age of 18 who arrive to Maaynei Hayeshua Medical center for any reason. The data will be transferred to a computerized data base and analyzed statistically.

Trial Health

50
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
300

participants targeted

Target at P75+ for all trials

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

August 1, 2008

Completed
3 days until next milestone

First Submitted

Initial submission to the registry

August 4, 2008

Completed
3 days until next milestone

First Posted

Study publicly available on registry

August 7, 2008

Completed
2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 1, 2010

Completed
Last Updated

August 7, 2008

Status Verified

August 1, 2008

Enrollment Period

2 years

First QC Date

August 4, 2008

Last Update Submit

August 6, 2008

Conditions

Keywords

incontinenceobstetric risk factorswomenof age 18above

Eligibility Criteria

Age18 Years+
Sexfemale
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

women of age 18 or above

You may qualify if:

  • women of age 18 or above

You may not qualify if:

  • women under the age of 18
  • men

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Central Study Contacts

Daphna H Weinstein, MD

CONTACT

Moshe Koller, MD

CONTACT

Study Design

Study Type
observational
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER

Study Record Dates

First Submitted

August 4, 2008

First Posted

August 7, 2008

Study Start

August 1, 2008

Primary Completion

August 1, 2010

Last Updated

August 7, 2008

Record last verified: 2008-08