NCT03064594

Brief Summary

This retrospective study is to find out the best way to treat patient with cornual pregnancy in the aspect of further pregnancy outcome.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
40

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Feb 2017

Geographic Reach
1 country

1 active site

Status
completed

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

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

February 9, 2017

Completed
Same day until next milestone

Study Start

First participant enrolled

February 9, 2017

Completed
18 days until next milestone

First Posted

Study publicly available on registry

February 27, 2017

Completed
8 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 12, 2017

Completed
1.1 years until next milestone

Study Completion

Last participant's last visit for all outcomes

November 2, 2018

Completed
Last Updated

February 15, 2019

Status Verified

February 1, 2019

Enrollment Period

8 months

First QC Date

February 9, 2017

Last Update Submit

February 12, 2019

Conditions

Cornual Pregnancy

Outcome Measures

Primary Outcomes (1)

  • pregnancy rate

    Comparison of pregnancy rates between the cornuostomy and wedge resection groups

    9 years

Study Arms (2)

cornuostomy

cornuostomy

Procedure: Cornual pregnancy

wedge resection

wedge resection

Interventions

Cornual pregnancyPROCEDURE

we will get the information of operative time, blood loss and postoperative pregnancy and delivery rate.

cornuostomy

Eligibility Criteria

Age20 Years+
Sexfemale
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

the cases with cornual pregnancy

You may qualify if:

  • All women with cornual pregnancy who were admitted to the Department of Obstetrics and Gynecology of the Far Eastern Memorial Hospital for laparoscopic surgeries between January 2008 and June 2016 were enrolled

You may not qualify if:

  • The person who was pregnant at the time of the operation
  • After receiving IVF course of treatment
  • Patients with uterine horns undergoing open surgery

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Department of Obstetrics and Gynecology, Far-Eastern Memorial Hospital

New Taipei City, Banqiao, 22060, Taiwan

Location

MeSH Terms

Conditions

Pregnancy, Cornual

Condition Hierarchy (Ancestors)

Pregnancy, EctopicPregnancy ComplicationsFemale Urogenital Diseases and Pregnancy ComplicationsUrogenital Diseases

Study Design

Study Type
observational
Observational Model
CASE CONTROL
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Chief, Department of Obstetrics & Gynecology

Study Record Dates

First Submitted

February 9, 2017

First Posted

February 27, 2017

Study Start

February 9, 2017

Primary Completion

October 12, 2017

Study Completion

November 2, 2018

Last Updated

February 15, 2019

Record last verified: 2019-02

Locations

TW(1)