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Immediate Post-placental Insertion of IUCD During Cesarean Delivery Versus 6 Week Post-Cesarean Insertion

NCT03404622 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 200

Last updated 2018-01-29

No results posted yet for this study

Summary

The aim of current study is to compare the rates of IUCD expulsion and complications in immediate post-placental insertion versus delayed IUCD insertion (6-weeks after cesarean delivery)

Conditions

  • Mechanical Complication of Intrauterine Device

Interventions

DRUG

IUCD

IUCD will be inserted in 100 women post placental removal and will be inserted in anther 100 women after six weeks post cesarean delivery

Sponsors & Collaborators

  • ALshaimaa Aboalhassan Ali

    lead OTHER

Principal Investigators

  • Yasser M Aboutalib, MD · Ain Shams University

  • Ahmed S AbdelHamid, MD · Ain Shams University

  • ALshaimaa A Ali, MBBch · Ain Shams University

  • Haitham Torky, MD · Ain Shams University

Study Design

Allocation
RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
DOUBLE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2016-09-20
Primary Completion
2016-12-20
Completion
2017-12-20
FDA Drug
Yes

Countries

  • Egypt

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 NCT03404622 on ClinicalTrials.gov