The Use of Levonorgestrel-Releasing Device (Metraplant-E) in the Treatment of Dysfunctional Uterine Bleeding

Ain Shams Maternity Hospital

Status and phase

Completed

Phase 2

Phase 1

Conditions

Dysfunctional Uterine Bleeding

Treatments

Device: Metraplant-E levonorgestrel-releasing intrauterine device

Study type

Interventional

Funder types

Other

Identifiers

NCT02326922

AAAM1983

Details and patient eligibility

About

Research hypothesis: Release of levonorgestrel from Metraplant-E levonorgestrel releasing intrauterine contraceptive device is inadequate to be used as a medical line of treatment of dysfunctional uterine bleeding.

The investigators aim to evaluate the therapeutic effect of the intrauterine system (Metraplant-E) in the treatment of dysfunctional uterine bleeding.

Full description

Primary outcome : The investigators aim to evaluate the short term release of levonorgestrel from the Metraplant-E levonorgestrel releasing intrauterine contraceptive devices (IUCDs). This is in a trial to determine to what extent the intrauterine release of levonorgestrel would reduce MBL in women with menorrhagia and if the treatment would increase the body iron stores and the degree of patient satisfaction and acceptability of treatment for the patients with dysfunctional uterine bleeding. This will be conducted through a questionnaire offered to the women participating in this study which is designed on Likert scale.

Secondary outcome:

Endometrial biopsy prior to and 6 months after the insertion of the intrauterine system (Metraplant-E).
Haemoglobin level measurement in gm/dl and serum ferritin level on same occasions as when endometrial biopsy is done.
The amount of monthly menstrual blood loss after the insertion the Metraplant-E levonorgestrel releasing intrauterine contraceptive devices using the following scores: bleeding index,total bleeding score and Pictorial blood loss assessment chart (PBAC).

Inclusion criteria:

Women seeking contraception.
Women with history of menorrhagia.
Pre and perimenopausal women who are married or previously married.
Failure of other medical treatment to control menorrhagia such as hemostatics.
Women who did not tolerate copper IUD (intrauterine device) due to increased amount of menstrual blood loss which could lead to anemia.

Enrollment

61 patients

Sex

Female

Ages

18 to 55 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Women seeking contraception.
Women with history of menorrhagia.
Pre and perimenopausal women who are married or previously married.
Failure of other medical treatment to control menorrhagia such as hemostatics.
Women who did not tolerate copper IUD due to increased amount of menstrual blood loss which could lead to anemia.

Exclusion criteria

History of ectopic pregnancy .
Pregnancy or suspicion of pregnancy.
Congenital or acquired uterine anomaly including fibroids if they distort the uterine cavity.
Acute pelvic inflammatory disease
Postpartum endometritis or infected abortion in the past 3 months.
Known or suspected uterine or cervical neoplasia or unresolved, abnormal Pap smear.
Genital bleeding of unknown etiology.
Untreated acute cervicitis or vaginitis, including bacterial vaginosis or other lower genital tract infections, until infection is controlled.
Acute liver disease or liver tumor (benign or malignant).
Conditions associated with increased susceptibility to infections with microorganisms. Such conditions include, but are not limited to, leukemia, acquired immune deficiency syndrome (AIDS), and I.V. drug abuse.
A previously inserted IUD that has not been removed.
Hypersensitivity to any component of this product.
Women taking anticoagulants
Women with coagulopathies due to thrombocytopenia or platelets dysfunction.
Known or suspected carcinoma of the breast.