PostPlacental IUD Insertion

Status

Completed

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT02679820

Enrollment

500

Registered

2016-02-10

Start date

2016-01-31

Completion date

2018-12-31

Last updated

2019-01-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Contraception

Brief summary

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

Interventions

DEVICECopper T intrauterine device

Study design

Allocation

RANDOMIZED

Intervention model

PARALLEL

Primary purpose

PREVENTION

Masking

NONE

Eligibility

Sex/Gender

FEMALE

Age

20 Years to 45 Years

Healthy volunteers

Yes

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.

Design outcomes

Primary

Measure	Time frame
Expulsion rate	6 months
The percentage of females seeking contraception	6 months

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 17, 2026