NCT03688581

Brief Summary

The main objective is to assess the knowledge of women seeking abortion about emergency contraception. The secondary objectives are to evaluate the use of emergency contraception among women seeking abortion and to identify barriers to the efficacy and use of emergency contraception in these women.

Trial Health

43
At Risk

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
250

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Jul 2018

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
unknown

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

Study Start

First participant enrolled

July 1, 2018

Completed
3 months until next milestone

First Submitted

Initial submission to the registry

September 26, 2018

Completed
2 days until next milestone

First Posted

Study publicly available on registry

September 28, 2018

Completed
9 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 1, 2019

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

July 1, 2019

Completed
Last Updated

April 18, 2019

Status Verified

September 1, 2018

Enrollment Period

1 year

First QC Date

September 26, 2018

Last Update Submit

April 16, 2019

Conditions

Abortion

Keywords

AbortionEmergency contraceptionEmergency pillPerception of pregnancy riskContraceptive failure

Outcome Measures

Primary Outcomes (1)

  • Assessment of women's knowledge of contraceptive methods through a questionnaire

    1 hour after consultation for abortion

Eligibility Criteria

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

woman seeking an abortion at the Orthogeny Center in University Hospitals of Strasbourg

You may qualify if:

  • women aged over eighteen years old
  • the patient agreed that her questionnaire data should be collected and analyzed for this research.
  • women who are able to read and write French
  • woman seeking an abortion at the Orthogeny Center in University Hospitals of Strasbourg

You may not qualify if:

  • refusal to participate in the study

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Service de Gynécologie - CMCO

Strasbourg, 67303, France

RECRUITING

Central Study Contacts

Karima BETTAHAR, MD

CONTACT

33 3 69 55 34 53karima.bettahar@chru-strasbourg.fr

Eva TILLY

CONTACT

33 3 69 55 34 53evatly67@gmail.com

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
OTHER
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

September 26, 2018

First Posted

September 28, 2018

Study Start

July 1, 2018

Primary Completion

July 1, 2019

Study Completion

July 1, 2019

Last Updated

April 18, 2019

Record last verified: 2018-09

Locations

FR(1)