Effect of propolis in pain of Endometriosis
Phase 3
Recruiting
- Conditions
- Condition 1: Endometriosis of pelvic peritoneum. Condition 2: Endometriosis of rectovaginal septum and vagina.Endometriosis of pelvic peritoneumEndometriosis of rectovaginal septum and vaginaN80.3N80.4
- Registration Number
- IRCT20141230020486N5
- Lead Sponsor
- Mashhad University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 40
Inclusion Criteria
All patients with a definite diagnosis of endometriosis by imaging and have pain due to endometriosis
Age between 20-45 years old
Use of standard progesterone hormone treatments
Not using NSAID medications
Not refer for infertility treatment
BMI between 18.5 to 27.5
Not taking food supplements
Obtaining the patient's informed consent
Exclusion Criteria
Use of hormonal contraception and IUD during the last 3 months
Pregnancy or breastfeeding in the last 3 months
The presence of any physical and mental disease
Drug sensitivity to propolis
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Endometriosis pain. Timepoint: Before the intervention and 4months after the intervention. Method of measurement: Visual Analogue Scale (VAS).
- Secondary Outcome Measures
Name Time Method