What is the Knowledge and Use of Emergency Contraception
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The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. |
| ClinicalTrials.gov Identifier: NCT03688581 |
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Recruitment Status : Unknown
Verified September 2018 by University Hospital, Strasbourg, France.
Recruitment status was: Recruiting
First Posted : September 28, 2018
Last Update Posted : April 18, 2019
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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.
| Condition or disease |
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| Abortion |
| Study Type : | Observational |
| Estimated Enrollment : | 250 participants |
| Observational Model: | Cohort |
| Time Perspective: | Other |
| Official Title: | What is the Knowledge and Use of Emergency Contraception for Women Who Are Seeking Abortion in University Hospitals of Strasbourg |
| Actual Study Start Date : | July 1, 2018 |
| Estimated Primary Completion Date : | July 2019 |
| Estimated Study Completion Date : | July 2019 |
- Assessment of women's knowledge of contraceptive methods through a questionnaire [ Time Frame: 1 hour after consultation for abortion ]
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.
| Ages Eligible for Study: | 18 Years and older (Adult, Older Adult) |
| Sexes Eligible for Study: | Female |
| Sampling Method: | Non-Probability Sample |
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
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03688581
| Contact: Karima BETTAHAR, MD | 33 3 69 55 34 53 | karima.bettahar@chru-strasbourg.fr | |
| Contact: Eva TILLY | 33 3 69 55 34 53 | evatly67@gmail.com |
| France | |
| Service de Gynécologie - CMCO | Recruiting |
| Strasbourg, France, 67303 | |
| Contact: Karima BETTAHAR, MD 33 3 69 55 34 53 karima.bettahar@chru-strasbourg.fr | |
| Contact: Eva TILLY 33 3 69 55 34 53 evatly67@gmail.com | |
| Principal Investigator: Karima BETTAHAR, MD | |
| Sub-Investigator: Catherine BURGY, Wise woman | |
| Sub-Investigator: Eva TILLY | |
| Responsible Party: | University Hospital, Strasbourg, France |
| ClinicalTrials.gov Identifier: | NCT03688581 |
| Other Study ID Numbers: |
7116 |
| First Posted: | September 28, 2018 Key Record Dates |
| Last Update Posted: | April 18, 2019 |
| Last Verified: | September 2018 |
| Studies a U.S. FDA-regulated Drug Product: | No |
| Studies a U.S. FDA-regulated Device Product: | No |
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Abortion Emergency contraception Emergency pill Perception of pregnancy risk Contraceptive failure |
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Emergencies Disease Attributes Pathologic Processes |

