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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03688581
Other study ID # 7116
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date July 1, 2018
Est. completion date July 2019

Study information

Verified date September 2018
Source University Hospital, Strasbourg, France
Contact Karima BETTAHAR, MD
Phone 33 3 69 55 34 53
Email karima.bettahar@chru-strasbourg.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial 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.


Recruitment information / eligibility

Status Recruiting
Enrollment 250
Est. completion date July 2019
Est. primary completion date July 2019
Accepts healthy volunteers
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria:

- 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

Exclusion Criteria:

- refusal to participate in the study

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
France Service de Gynécologie - CMCO Strasbourg

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Strasbourg, France

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Assessment of women's knowledge of contraceptive methods through a questionnaire 1 hour after consultation for abortion
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