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Management of Uterine Leiomyomata and Adenomyosis

A

Ahmed Ali Mahmoud

Status

Unknown

Conditions

Abnormal Uterine Bleeding

Treatments

Drug: Norethisterone acetate

Study type

Observational

Funder types

Other

Identifiers

NCT05153928
12091984

Details and patient eligibility

About

  1. to determine the role of hysteroscopy and guided biopsy to differentiate between submucosal fibroids and adenomyosis confirmed by histopathological examination
  2. to evaluate the efficacy of norethisterone in the treatment of symptomatic adenomyosis and leiomyoma

Full description

The aim of the present study is:

  1. to determine the role of hysteroscopy and guided biopsy to differentiate between submucosal fibroids and adenomyosis confirmed by histopathological examination
  2. to evaluate the efficacy of norethisterone in the treatment of symptomatic adenomyosis and leiomyoma

Enrollment

100 estimated patients

Sex

Female

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • (1) age≥30 years; (4) dysmenorrhea, adenomyosis-associated chronic pain, and/or menorrhagia.

(3) regular menstrual cycles before administration of norethisterone; (4) no other treatment for adenomyosis/leiomyomatosis at least for 3 months biopsies and histopathology for operated patients;

Exclusion criteria

  • (1) pregnant and/or breast-feeding women (2) patients with a ovarian neoplasm, benign ovarian cyst including endometrioma, pelvic inflammatory disease or other endocrine diseases.

Trial design

100 participants in 2 patient groups

fibroid cases
Description:
Norethisterone acetate for 5 months
Treatment:
Drug: Norethisterone acetate
adenomyosis
Description:
Norethisterone acetate for 5 months
Treatment:
Drug: Norethisterone acetate

Trial contacts and locations

2

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Central trial contact

ahmed Al Dr, Msc; Ahmed Ali

Data sourced from clinicaltrials.gov

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