Post Abortion IUD & Recurrent Abortion 2005-2006
|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|
- The proportion of repeat abortions at five years from the index abortions [ Time Frame: 5 years ]
- Correlation of repeat and index abortions with obstetrical, demographic and contraceptive history factors. [ Time Frame: 2 months ]
|Study Start Date:||July 2012|
|Study Completion Date:||December 2012|
|Primary Completion Date:||December 2012 (Final data collection date for primary outcome measure)|
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
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.
Please refer to this study by its ClinicalTrials.gov identifier: NCT01776957
|Principal Investigator:||Wendy Norman, Dr.||University of British Columbia|