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Clinical Trials/NCT01223521
NCT01223521
Completed
Not Applicable

Systematic Provision of Intrauterine Contraception After First Trimester Abortion - Effects on Quality of Life and Risk of Repeat Abortion. A Randomized, Prospective Trial.

Helsinki University Central Hospital1 site in 1 country748 target enrollmentSeptember 2010
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ConditionsContraception

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Contraception
Sponsor
Helsinki University Central Hospital
Enrollment
748
Locations
1
Primary Endpoint
Number of repeat abortions
Status
Completed
Last Updated
7 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSitesSimilar Trials

Overview

Brief Summary

A randomized prospective study on the effects of immediate provision of intrauterine contraception after first trimester induced abortion - effects on repeat abortions and quality of life.

Registry
clinicaltrials.gov
Start Date
September 2010
End Date
March 2018
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Elina Pohjoranta

MD

Helsinki University Central Hospital

Eligibility Criteria

Inclusion Criteria

  • •Duration of pregnancy \< 12 weeks.
  • •Age ≥18 years

Exclusion Criteria

  • •Contraindication for spiral insertion: uterine anomaly, infection, copper allergy (Cu-IUD).

Outcomes

Primary Outcomes

Number of repeat abortions

Time Frame: 5 years

Number of subsequent abortions during five years follow-up time.

Study Sites (1)

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