PostPlacental IUD Insertion

The immediate post cesarean section IUD insertion is a further step towards spreading more compliance to females in developing countries, with rapid increase in population size

Completed

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Key information

Conditions

Contraception

Age range

20 year–45 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Kasr el aini hospital

Cairo, 12211, Egypt

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Females desiring contraception by using intrauterine device following their vaginal delivery or cesarean section

Exclusion criteria

refusal to participate in the study
desiring other methods of contraception
will not use any method of contraception
has a contraindication for the use of IUD as bicornuate or septate uterus, sub mucous myomas, etc.

Treatment and study plan

Copper T intrauterine device

Device

Other names: copper T IUD

Primary outcomes

Expulsion rate

Time frame: 6 months
The percentage of females seeking contraception

Time frame: 6 months

Sponsors and collaborators

Lead sponsor

Woman's Health University Hospital, Egypt

Other

Registry information

Important dates

Study start: 2016
Primary completion: 2018
Study completion: 2018
First posted: Feb 10, 2016
Registry last updated: Jan 9, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.

Completed