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Emergency Contraception (ECP): Reducing Unintended Pregnancies - Article


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Contraception

Condom; Condoms




Clinical Trial: Emergency Contraception (ECP): Reducing Unintended Pregnancies

This study has been completed.

Sponsored by: National Institute of Child Health and Human Development (NICHD)
Information provided by: National Institute of Child Health and Human Development (NICHD)

Purpose

Emergency contraception is a method of birth control that can be used up to three days after sexual intercourse. Emergency contraceptive pills (ECPs) can be given to a woman before she needs them (advance provision) or when she needs them (emergency provision). This study will compare these two methods of providing ECPs.

Condition Treatment or Intervention Phase
Contraception
Pregnancy
 Drug: emergency contraception (estrogen/progesterone)
Phase IV

MedlinePlus consumer health information 

Study Type: Interventional
Study Design: Prevention, Non-Randomized, Open Label, Active Control, Factorial Assignment, Efficacy Study

Official Title: A Second Chance with Emergency Contraception (ECP): Reducing Unintended Pregnancy

Further Study Details: 

Expected Total Enrollment:  1100

Study start: June 2001;  Study completion: May 2004

ECPs can give women a “second chance” to prevent an unintended pregnancy that might arise because of lack or improper/defective use of contraceptives. By using ECP, a woman can reduce her risk of pregnancy by at least 75%; however, there is little information on what distribution patterns and other factors are most likely to encourage ECP use. This study will compare the use and cost of two ECP distribution patterns: advance provision and emergency provision. It will also identify environmental, situational, and behavioral factors associated with ECP acceptance and use.

Participants in this study will be recruited from four family planning clinics in the Philadelphia area and five family planning clinics in the Pittsburgh area. Participants from the Philadelphia clinics will be given ECPs as part of a regular clinic visit (advance provision); participants from the Pittsburgh clinics will be given ECPs on an emergency basis (emergent provision). Each participant will complete a short intake form and will be issued a pager. Participants will be paged every month over an 18-month period as a reminder to respond to a short automated telephone survey on ECP, contraceptives, and pregnancy status. Approximately half of the participants will be randomly selected to participate in in-depth interviews at study entry and Months 9 and 18. Clinic visit data will augment the surveys to verify use of the clinic and contraceptive method and to develop cost data.

Eligibility

Ages Eligible for Study:  15 Years   -   39 Years,  Genders Eligible for Study:  Female

Accepts Healthy Volunteers

Criteria

Inclusion Criteria

  • Patient at a participating clinic

Exclusion Criteria

  • Pregnant
  • Medical or surgical procedure preventing pregnancy (e.g., tubal ligation, hysterectomy)
  • Norplant or IUDs
  • Desires to become pregnant

Location Information


Pennsylvania
      Family Planning Council, Philadelphia,  Pennsylvania,  19102,  United States

      Family Health Council, Pittsburgh,  Pennsylvania,  15222,  United States

Study chairs or principal investigators

Paul G Whittaker, D.Phil.,  Principal Investigator

More Information

Study ID Numbers:  HD38515
Record last reviewed:  July 2003
Last Updated:  October 13, 2004
Record first received:  August 21, 2003
ClinicalTrials.gov Identifier:  NCT00067509
Health Authority: United States: Federal Government
ClinicalTrials.gov processed this record on 2005-04-08


Source: ClinicalTrials.gov
Cache Date: April 9, 2005

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December 4, 2008



Page Updated: October 3, 2005
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