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Postplacental Intrauterine Device Insertion: A Mixed Methods Assessment of Women's Experience

NCT02312726 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 135

Last updated 2016-04-04

Study results available
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Summary

The primary objective of this mixed methods pilot study is to understand women's experiences with postplacental intrauterine device (IUD) insertion through postpartum semi-structured interviews. For secondary objectives, the investigators will collect visual analog scale (VAS) and verbal rating score (VRS) data on women's pain experienced just before and immediately after IUD insertion. The investigators will perform postpartum interviews in each group until we reach thematic saturation. The investigators will recruit at least 60 women (30 each in the epidural and no epidural group) from the University of New Mexico Hospital (UNMH) affiliated antenatal clinics to conduct our quantitative data analysis.

Conditions

  • Contraception

Interventions

PROCEDURE

Postplacental IUD insertion

Postplacental IUD insertion using the standardized ring forceps technique (Speroff and Mishell 2008) under ultrasound guidance, within 10-30 minutes of vaginal delivery.

Sponsors & Collaborators

Principal Investigators

  • Rameet H Singh, MD, MPH · UNM OB GYN Division of Family Planning

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2013-11-30
Primary Completion
2015-03-31
Completion
2015-03-31

Countries

  • United States

Study Locations

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Entities

Companies

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 NCT02312726 on ClinicalTrials.gov