NCT04830007

Brief Summary

The study will be offered to all women who are consultant for an abortion plan are seen in consultation at the orthogeny center where the study will be conducted. Of these 700 women, about 10% will not agree to participate in the study and 10% will not meet the inclusion criteria. Thus it's plane to include 560 patients in the study.

Trial Health

33
At Risk

Trial Health Score

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

Trial has exceeded expected completion date
Trial recruitment is currently suspended
Enrollment
560

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Nov 2022

Geographic Reach
1 country

1 active site

Status
suspended

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 11, 2021

Completed
2 months until next milestone

First Posted

Study publicly available on registry

April 2, 2021

Completed
1.6 years until next milestone

Study Start

First participant enrolled

November 1, 2022

Completed
Same day until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 1, 2022

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

November 1, 2022

Completed
Last Updated

February 1, 2022

Status Verified

January 1, 2022

Enrollment Period

Same day

First QC Date

February 11, 2021

Last Update Submit

January 31, 2022

Conditions

Pregnancy, Unwanted

Keywords

ContraceptionAbortionUnplanned pregnancyUnintended pregnancy

Outcome Measures

Primary Outcomes (1)

  • Association between absence of contraception and socio-demographic factors, characteristics of pregnancy abortion and medical follow-up

    Statistically significant association between the absence of contraception in patients consulting for a voluntary termination of pregnancy and socio-demographic factors, characteristics of voluntary termination of pregnancy abortion and characteristics related to medical follow-up

    1 hour

Secondary Outcomes (7)

  • Prescription and dispensing of contraception

    1 hour

  • Existence of family planning centers

    1 hour

  • Emergency contraception

    1 hour

  • Price and reimbursement of condoms

    1 hour

  • Knowledge of conception

    1 hour

  • +2 more secondary outcomes

Eligibility Criteria

Age18 Years+
Sexfemale(Gender-based eligibility)
Gender Eligibility DetailsOnly pregant women
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Protocol proposed to woman who wanted a voluntary termination of pregnancy

You may qualify if:

  • woman of 18 years of age or older;
  • Being French-speaking;
  • request for a medical or instrumental voluntary termination of pregnancy
  • No opposition to participation in the protocol
  • Be affiliated with a social security plan

You may not qualify if:

  • desired pregnancy

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

CHI Villeneuve St Georges

Villeneuve-Saint-Georges, France

Location

Study Design

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

Study Record Dates

First Submitted

February 11, 2021

First Posted

April 2, 2021

Study Start

November 1, 2022

Primary Completion

November 1, 2022

Study Completion

November 1, 2022

Last Updated

February 1, 2022

Record last verified: 2022-01

Locations

FR(1)