NCT01776957

Brief Summary

The rate of repeat abortions will be lowest in those women who choose immediate insertion of an IUD post-abortion versus those who immediately choose oral contraceptive pills and those who indicate all other contraceptive choices including no contraception The provision by the health system of IUDs for immediate insertion will result in the lowest health system costs.

Trial Health

55
Monitor

Trial Health Score

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

Enrollment
1,308

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Jul 2012

Shorter than P25 for all trials

Status
terminated

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

July 1, 2012

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2012

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2012

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

January 21, 2013

Completed
7 days until next milestone

First Posted

Study publicly available on registry

January 28, 2013

Completed
Last Updated

May 4, 2018

Status Verified

May 1, 2018

Enrollment Period

5 months

First QC Date

January 21, 2013

Last Update Submit

May 1, 2018

Conditions

Induced Abortion

Keywords

Abortion rateIntrauterine device

Outcome Measures

Primary Outcomes (1)

  • The proportion of repeat abortions at five years from the index abortions

    5 years

Secondary Outcomes (1)

  • Correlation of repeat and index abortions with obstetrical, demographic and contraceptive history factors.

    2 months

Study Arms (1)

IUD

Repeat abortion rate in women receiving IUDs immediately post-abortion

Device: Device: Intrauterine device (IUD)

Interventions

Device: Intrauterine device (IUD)DEVICE

Women choosing to have an intrauterine device (IUD) inserted immediately post-abortion

IUD

Eligibility Criteria

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

Female resident of Interior Health region seeking an abortion

You may qualify if:

  • Female resident of Interior Health region seeking an abortion between January 1, 2005 and December 31, 2006

You may not qualify if:

  • Women undergoing abortions for fetal genetic abnormalities

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Interventions

Intrauterine Devices

Intervention Hierarchy (Ancestors)

Contraceptive Devices, FemaleContraceptive DevicesEquipment and Supplies

Study Officials

  • Wendy Norman, Dr.

    University of British Columbia

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principle Investigator

Study Record Dates

First Submitted

January 21, 2013

First Posted

January 28, 2013

Study Start

July 1, 2012

Primary Completion

December 1, 2012

Study Completion

December 1, 2012

Last Updated

May 4, 2018

Record last verified: 2018-05