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NCT03688581 Clinical Trial

What is the Knowledge and Use of Emergency Contraception

Abortion Clinical Trial

Official title:
What is the Knowledge and Use of Emergency Contraception for Women Who Are Seeking Abortion in University Hospitals of Strasbourg

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
See also
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Completed NCT00986921 - Mifepristone Versus Laminaria Insertion for Cervical Preparation Prior to Surgical Abortion at 14-16 Weeks N/A
Completed NCT00769912 - Evaluation of of a Prefixed 50% N2O- 50%O2 Mixture in Legal Abortion Under Local Analgesia Phase 3
Completed NCT00235534 - Trial of Immediate Versus Delayed Initiation of Oral Contraceptive Pills After Abortion N/A
Completed NCT06178224 - Determining Beta-hCG Levels in Patients Through Alternative Sample Types
Completed NCT04181021 - Evaluation of Values Clarification and Attitude Transformation Workshops on Abortion and Family Planning Service Provision and Client Experience N/A
Completed NCT01799252 - Side Effects and Adherence Associated With Doxycycline Use Following Medical Abortion N/A
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Completed NCT02580175 - Surgical Evacuation of Abortion Under Ultrasonographic Guide Phase 2
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Completed NCT01945385 - Impact of Video Intervention on Postabortal Uptake of Long Acting Reversible Contraception (LARC) N/A
Terminated NCT01436266 - Effect of Preoperative Buccal Misoprostol on Blood Loss in Second-trimester Dilation and Evacuation Abortion Phase 3
Completed NCT03227614 - Friends/Family in the Abortion Procedure Room (FAIR) N/A
Not yet recruiting NCT05471895 - Impact of Sexual Violence on the Incidence of Voluntary Termination of Pregnancy in La Réunion
Completed NCT05688228 - Voluntary Interruption of Pregnancy on Women's Sexuality
Completed NCT03136068 - Intrafetal Digoxin as an Adjuvant for Dilation and Evacuation at 20 to 24 Weeks' Gestation Phase 4
Completed NCT04651166 - Effect of Prophylactic Tranexamic Acid on Bleeding Outcomes for Dilation and Evacuation Phase 2
Recruiting NCT05645614 - Anxiety and Pain During Intervention for Abortion Under Local Anesthesia
Completed NCT01807715 - Understanding Women's Contraceptive Expectations at the Time of a First Trimester Surgical Abortion