跳至主要内容
临床试验/NCT00433004
NCT00433004已完成4 期

A Pilot Randomized Control Trial of Advanced Supply of Levonorgestrel Emergency Contraception vs. Routine Postpartum Contraceptive Care in the Teenage Population

University of Pennsylvania1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2007年2月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
入组人数
50
试验地点
1
主要终点
PLAN B USE

研究概览

简要总结

This is a pilot randomized controlled trial to assess the effects of advanced supply of emergency contraception versus routine care in a teen postpartum population. The goals are to assess feasibility of recruiting and retaining postpartum teens; to obtain estimates of the prevalence of (use of Plan B, primary contraceptive continuation, unprotected intercourse exposure, and pregnancy rates), in postpartum teens given advanced supply of Plan B; to assess whether or not (lack of use of Plan B, contraceptive method non-continuation, and unprotected intercourse exposure), are surrogate markers for risk of unintended pregnancy.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Health Services Research
盲法
None

入排标准

年龄范围
14 Years 至 19 Years(Child, Adult)
性别
Female
接受健康志愿者

入选标准

  • English speaking
  • Aged 14-19 at enrollment
  • Immediately postpartum of a live infant
  • Planning to parent the baby
  • Desiring to delay another pregnancy for at least one year
  • General good health
  • Willing and able to follow the study protocol
  • Exclusion Criteria
  • Allergy to levonorgestrel
  • Current substance abuse
  • Plans for relocation outside of Philadelphia

排除标准

  • 未提供

研究组 & 干预措施

2

Active Comparator

Advance supply of emergency contraception is given

干预措施: Plan B (Levonorgestrel) (Drug)

结局指标

主要结局

PLAN B USE

时间窗: 1 year

ABILITY TO FOLLOW POSTPARTUM TEENS FOR 1 YEAR.

时间窗: 1 year

PREGNANCY RATES

时间窗: 1 year

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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