Overview

Evaluation of Using Dienogest and N-Acetyl Cysteine on the Volume of Uterine Leiomyoma

Status:
Recruiting
Trial end date:
2023-12-31
Target enrollment:
0
Participant gender:
Female
Summary
This 2 arm randomized clinical trial will assess the impact of Dienogest and N-Acetyl Cysteine on volume reduction of uterine leiomyoma
Phase:
Phase 2/Phase 3
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
Ain Shams University
Treatments:
Acetylcysteine
Dienogest
N-monoacetylcystine
Criteria
Inclusion Criteria:

1. Age: 20-45 years.

2. Women with uterine leiomyoma (sub-mucous, sub-serous or intramural) based on
transvaginal sonography criteria. Uterine fibroids most often appear as concentric,
solid, hypoechoic masses. This appearance results from the prevailing muscle, which is
observed at histologic examination. These solid masses absorb sound waves and
therefore cause a variable amount of acoustic shadowing.

3. Regular menstruation: regular period interval from 21 to 35 days.

Exclusion Criteria:

1. Pregnant or menopausal women.

2. History of malignancies, metabolic, hematologic, cardiac, thromboembolism, diabetes,
renal or hepatic diseases.

3. History of hormonal drug use or treatment for leiomyoma in the past 3 months.