Clinical Trials Directory

Trials / Unknown

UnknownNCT02465658

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

Status
Unknown
Phase
Study type
Observational
Enrollment
300 (estimated)
Sponsor
National Taiwan University Hospital · Academic / Other
Sex
Female
Age
20 Years
Healthy volunteers
Not accepted

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.

Detailed 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.

Conditions

Interventions

TypeNameDescription
OTHERMedical records were reviewed.retrospective study

Timeline

Start date
2015-03-01
Primary completion
2016-03-01
Completion
2016-03-01
First posted
2015-06-08
Last updated
2015-12-16

Locations

1 site across 1 country: Taiwan

Source: ClinicalTrials.gov record NCT02465658. Inclusion in this directory is not an endorsement.