Skip to main content
Clinical Trials/NCT03140800
NCT03140800
Unknown
Not Applicable

Intrauterine Contraceptive Device:Clinical and Sonographic Correlation in Patients Presenting With Bleeding

Assiut University0 sites60 target enrollmentJune 2017
ConditionsContraception

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Contraception
Sponsor
Assiut University
Enrollment
60
Primary Endpoint
The intrauterine device-Endometrial distance
Last Updated
9 years ago

Overview

Brief Summary

Intrauterine contraceptive device is one of the most efficient and reversible methods of birth control with low cost and long duration of use However, in the first year after insertion, between 5 and 15% of women will have their Intrauterine contraceptive device removed because of irregular uterine bleeding which have been attributed to the effect of contact between the device and the endometrium and even the pressure on the uterine muscle . The disharmonious relationship between the Intrauterine contraceptive device and the uterus is the cause of most of the bleeding complaints, so bleeding is related to improper position rather than the contraceptive method itself which should be excluded before abandoning the Intrauterine contraceptive device for any other method of birth control

Registry
clinicaltrials.gov
Start Date
June 2017
End Date
March 2019
Last Updated
9 years ago
Study Type
Observational
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

ESShafeek

Dr

Assiut University

Eligibility Criteria

Inclusion Criteria

  • patients using intrauterine contraceptive device complaining of bleeding

Exclusion Criteria

  • a-Associated uterine, cervical,or adenexal pathology b-Associated pelvic infection c-Generalized bleeding disorders d-Medications causing coagulation defects e-Medical disorders causing bleeding e.g hypertention f-Endocrine disorder as thyroid dysfunction g-Who refuse to share in the study

Outcomes

Primary Outcomes

The intrauterine device-Endometrial distance

Time Frame: 3 months

Similar Trials