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NCT02465658 Clinical Trial

Risk Factors for Co-existence of Cervical Elongation in Uterine Prolapse

Pelvic Organ Prolapse Clinical Trial

Official title:
Risk Factors for Co-existence of Cervical Elongation in Uterine Prolapse

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT02465658
Other study ID # 201503073RIND
Secondary ID
Status Recruiting
Phase N/A
First received June 4, 2015
Last updated December 15, 2015
Start date March 2015
Est. completion date March 2016

Study information
Verified date December 2015
Source National Taiwan University Hospital
Contact Ho-Hsiung Lin, MD,PhD
Phone 886-2-23123456
Email hhlin@ntuh.gov.tw
Is FDA regulated No
Health authority Taiwan: Ministry of Health and Welfare
Study type Observational

Clinical Trial Summary

The presence of co-existence of cervical elongation in women of uterine prolapse may decrease the patients' satisfaction of uterine-preservation surgery for uterine prolapse, and additional surgery, such as Manchester surgery, may be needed to solve the problem.Thus the aim of this study is to investigate the risk factors of co-existence of cervical elongation in uterine prolapse.

Description:

Purpose:

Thus the aim of this study is to investigate the risk factors of co-existence of cervical elongation in uterine prolapse.

Patients and Methods:

Between January 1994 and October 2014, all women underwent vaginal total hysterectomy in a medical center were enrolled in this study. Medical records were reviewed. Cervical elongation is defined as the presence of cervical length >3.38 cm or cervix to corpus ratio >0.79.

Expected Results:

The investigators will get the risk factors of co-existence of cervical elongation in uterine prolapse, and the result should be helpful for preoperative consultation, especially for uterine-preserving pelvic floor reconstruction surgery.

Recruitment information / eligibility
Status Recruiting
Enrollment 300
Est. completion date March 2016
Est. primary completion date March 2016
Accepts healthy volunteers No
Gender Female
Age group 20 Years and older
Eligibility Inclusion Criteria:

- All women with uterine prolapse underwent vaginal total hysterectomy

- > 20 years old.

Exclusion Criteria:

Study Design

Observational Model: Case-Only, Time Perspective: Retrospective

Related Conditions & MeSH terms

Intervention

Other:
• Medical records were reviewed.
retrospective study

Locations
Country Name City State
Taiwan Department of Obstetrics & Gynecology, National Taiwan University Hospital Taipei

Sponsors (1)
Lead Sponsor Collaborator
National Taiwan University Hospital

Country where clinical trial is conducted

Taiwan, 

Outcome
Type Measure Description Time frame Safety issue
Primary Factors associated with coexistent cervical elongation in cases with uterine prolapse Medical record review 1 day No
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