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Contraceptive Choice at the Time of Uterine Evacuation

NCT02836561 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 234

Last updated 2017-04-18

No results posted yet for this study

Summary

The goal of this project is to investigate whether a pre-visit telephone intervention could increase awareness of long-acting reversible contraception (LARC) availability at the time of uterine evacuation.

Conditions

  • Contraception

Interventions

OTHER

Telephone message

A pre-visit telephone intervention describing availability of long-acting reversible contraceptives at time of uterine evacuation

Sponsors & Collaborators

  • Planned Parenthood League of Massachusetts

    lead OTHER

Principal Investigators

  • Principal Investigator, MD · Planned Parenthood League of Massachusetts

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2016-07-31
Primary Completion
2017-04-30
Completion
2017-04-30

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02836561 on ClinicalTrials.gov