MedTrace Logo

Copper Intrauterine Device (IUD) Insertion at Cesarean Delivery

NCT01439802 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 90

Last updated 2023-04-07

Study results available
· View outcomes & findings →

Summary

The purpose of this study is to determine the expulsion rates of copper Intrauterine Devices (IUDs) placed at time of Cesarean Delivery.

Conditions

  • Intrauterine Device Expulsion

Interventions

DEVICE

Copper IUD placement at time Cesarean Delivery (Copper T 380A)

Placement of Paragard IUD at time of Cesarean Delivery

Sponsors & Collaborators

  • Albert Einstein College of Medicine

    lead OTHER

Principal Investigators

  • Amitasrigowri Murthy, MD · NYU School of Medicine

Study Design

Allocation
NON_RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
50 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2008-08-31
Primary Completion
2009-11-30
Completion
2010-05-31

Countries

  • United States

Study Locations

More Related Trials

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 NCT01439802 on ClinicalTrials.gov