The effect of Achillea Cretica herbal medicine on pain and size of endometrial lesions in patients.

Phase 3

Recruiting

• Conditions: Endometriosis.; Endometriosis

• Registration Number: IRCT20220408054455N1
• Lead Sponsor: Tehran University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 29 August 2022

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: 80

Inclusion Criteria

Women 18 to 45 years old with pain associated with endometriosis

Exclusion Criteria

Pregnancy
Breastfeeding
The need for endometriosis surgery treatment
Amenorrhea within 3 months prior to enrollment
Previous use of hormonal agents (e.g., gonadotropin agonists less than 6 months ago, progesterone or danazol less than 3 months ago, or oral contraceptives 1 month before screening)
Abnormal findings in gynecological examination
Risk factors for decreased bone density (e.g., family history of osteoporosis or use of anticonvulsants or corticosteroids)

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Degree of dysmenorrhea using visual pain ruler. Timepoint: At the beginning of the study and three months after starting treatment. Method of measurement: Using visual pain ruler.;Degree of dyspareunia using visual pain ruler. Timepoint: At the beginning of the study and three months after starting treatment. Method of measurement: Using pain ruler.;Degree of pelvic pain using pain ruler. Timepoint: At the beginning of the study and three months after starting treatment. Method of measurement: Using pain ruler.;Size change of Endometriosis lesions by Sonography or Laparascopy. Timepoint: At the beginning of the study and three months after starting treatment. Method of measurement: By performing ultrasound or diagnostic laparoscopy.;Number Change of endometriosis lesions by performing ultrasound. Timepoint: At the beginning of the study and three months after starting treatment. Method of measurement: By performing ultrasound or diagnostic laparoscopy.