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LNG-IUS for Treatment of Dysmenorrhea

Levonorgestrel-releasing Intrauterine System Compared to Low Dose Combined Oral Contraceptive Pills for Treatment of Adenomyosis: a Randomized Controlled Trial

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01601366
Acronym
LNGIUSAD
Enrollment
62
Registered
2012-05-18
Start date
2012-04-30
Completion date
2015-04-30
Last updated
2017-11-22

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

Conditions

Adenomyosis

Keywords

Adenomyosis, Intrauterine levonorgestrel, Dysmenorrhea, Oral contraceptives, Uterus

Brief summary

Adenomyosis is a disease entity diagnosed when endometrial glands and stroma deep in the myometrium are associated with surrounding myometrial hypertrophy. The finding classically associated with adenomyosis is excessive uterine bleeding accompanied by worsening dysmenorrhea. The advent of endovaginal US has substantially improved the ability to diagnose adenomyosis. Different US features of adenomyosis have been reported, including uterine enlargement not explainable by the presence of leiomyomas, asymmetric thickening of the anterior or posterior myometrial wall, lack of contour abnormality or mass effect, heterogeneous poorly circumscribed areas within the myometrium, anechoic lacunae or cysts of varying sizes, and increased echotexture of the myometrium. Transvaginal power Doppler application is useful in studying the vascular tree of adenomyosis and can aid clinicians in planning the most appropriate therapeutic strategy. The differential diagnosis using power Doppler sonography is based on vascular characteristics. Adenomyosis is characterized by a preserved vascular texture supply that results in dilated spiral arteries running perpendicular toward the myometrium into the endometrial surface. Leiomyomata exhibits a vascular tree that typically circumscribes the solid mass. 2D transvaginal power Doppler angiography should be used to improve diagnostic sensitivity and facilitate appropriate therapeutic intervention. The levonorgestrel-releasing intrauterine system (IUS), Mirena, has been approved in Europe for contraception since 1990. Because of the suppressive effect of levonorgestrel on the endometrium, Mirena has also been proven to be effective for the management of menorrhagia and dysmenorrhea, and as a progestin component in postmenopausal hormone therapy. It was introduced in Taiwan in 1995 as an alternative therapy for idiopathic menorrhagia. Many cases of menorrhagia are caused by adenomyosis, and Mirena was, therefore, introduced for the treatment of adenomyosis in Taiwan. The current study is designed to evaluate the best treatment modality for treatment of adenomyosis clinical by assessment of dysmenorrhea and or chronic pelvic pain by visual analogue scale and menstrual blood loss by menstrual diary, imaging by ultrasound and Doppler indices.

Interventions

DEVICELNG-IUS

The study includes 2 treatment groups: Group I the LNG-IUS group where they will have a LNG IUS inserted for them

Group II: will recite combined oral contraceptives for 6 months

Sponsors

Omar Mamdouh Shaaban
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
20 Years to 45 Years
Healthy volunteers
Yes

Inclusion criteria

1. Women have dysmenorrhoea and/or chronic pelvic pain secondary to adenomyosis. 2. Planning for birth spacing for at least 2 years. 3. Patient aged between 20-45 years old. 4. Ultrasonographic and Doppler examination suggestive of adenomyosis. 5. Living in a nearby area to make follow-up reasonably possible.

Exclusion criteria

1. Pregnancy 2. Evidence of defective coagulation. 3. History or evidence of malignancy. 4. Hyperplasia in the endometrial biopsy. 5. Incidental adnexal abnormality on ultrasound. 6. Contraindications to COCs. 7. Absolute contraindication of LNG-IUS insertion. 8. Previous endometrial ablation or resection 9. Uninvestigated postcoital bleeding 10. Untreated abnormal cervical cytology

Design outcomes

Primary

MeasureTime frame
Visual analogue score (VAS) for dysmenorrhea or chronic pelvic pain will be measure before after use LNG_IUS and COCs.6 month

Secondary

MeasureTime frame
Menstrual blood loss: assessment of blood loss, measured at the beginning of intervention and for 3 months6 month

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026