Trial record 2 of 364 for:    abortion

Post Abortion IUD & Recurrent Abortion 2005-2006

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
University of British Columbia
ClinicalTrials.gov Identifier:
NCT01776957
First received: January 21, 2013
Last updated: February 1, 2013
Last verified: February 2013
  Purpose

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.


Condition Intervention
Induced Abortion
Device: Device: Intrauterine device (IUD)

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Retrospective
Official Title: Preventing Repeat Abortion: Is the Immediate Insertion of Intrauterine Devices Post-abortion a Cost-effective Option Associated With Fewer Repeat Abortions? Findings From 2005-2006 Data

Further study details as provided by University of British Columbia:

Primary Outcome Measures:
  • The proportion of repeat abortions at five years from the index abortions [ Time Frame: 5 years ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • Correlation of repeat and index abortions with obstetrical, demographic and contraceptive history factors. [ Time Frame: 2 months ] [ Designated as safety issue: No ]

Enrollment: 1308
Study Start Date: July 2012
Study Completion Date: December 2012
Primary Completion Date: December 2012 (Final data collection date for primary outcome measure)
Groups/Cohorts Assigned Interventions
IUD
Repeat abortion rate in women receiving IUDs immediately post-abortion
Device: Device: Intrauterine device (IUD)
Women choosing to have an intrauterine device (IUD) inserted immediately post-abortion

Detailed Description:

The investigators intend to demonstrate whether there are statistically significant differences in the rates of repeat abortions between three groups: 1. women choosing to have an intrauterine device (IUD) inserted immediately post-abortion, 2. those choosing to begin oral contraceptives immediately post-abortion, and 3. all other choices for post abortion contraception including those stating an intention to obtain contraceptives at a later time or from an alternate location or to use no contraception. This data will then be used to conduct a cost-effectiveness analysis of health system provision for cost-free IUDs post-abortion. Thus, if providing a free IUD immediately post-abortion significantly reduces the rate of repeat abortions, it may be more cost- effective for health system services to provide free IUDs at abortion clinics than to field the costs associated with a higher rate of repeat abortions.

The researchers will conduct a retrospective observational cohort study by chart review. The researchers propose to review the charts of women undergoing abortions between January 1, 2005 and December 31, 2006 at Kelowna General Hospital's Women's Services Clinic. The researchers will record the following data from each chart: age, parity, gestational age, date of index therapeutic abortion (TA), dates of subsequent TAs, contraception used at the time of the index conception, contraceptive method chosen post-abortion, and outcome of follow-up at two weeks, such as expulsion of IUD. The researchers will also record the recurrent pregnancy rates.

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Female
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample
Study Population

Female resident of Interior Health region seeking an abortion

Criteria

Inclusion Criteria:

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

Exclusion Criteria:

  • Women undergoing abortions for fetal genetic abnormalities
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01776957

Sponsors and Collaborators
University of British Columbia
Investigators
Principal Investigator: Wendy Norman, Dr. University of British Columbia
  More Information

No publications provided

Responsible Party: University of British Columbia
ClinicalTrials.gov Identifier: NCT01776957     History of Changes
Other Study ID Numbers: H12-00829
Study First Received: January 21, 2013
Last Updated: February 1, 2013
Health Authority: Canada: Health Canada

Keywords provided by University of British Columbia:
Abortion rate
Intrauterine device

Additional relevant MeSH terms:
Abortion, Habitual
Abortion, Spontaneous
Pregnancy Complications

ClinicalTrials.gov processed this record on April 16, 2014