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The comparison of treatment with dienogest and contraceptive oral pills on the improvement of pain, and quality of life in surgery patients with advanced endometriosis

Phase 1
Conditions
Advanced endometriosis.
Endometriosis
Registration Number
IRCT20191011045063N1
Lead Sponsor
Iran University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
108
Inclusion Criteria

Early diagnosis of endometriosis and chronic pelvic pain associated with endometriosis
Patients with advanced endometriosis who underwent surgery
Age 18 - 45 years
Body mass index (BMI) 18.5 – 29.9 kg/m2;
No gynecological malignancy
No contraindications to OCP or dienogest
No plans of pregnancy in the near
No underlying diseases

Exclusion Criteria

Personal dissatisfaction for inclusion in the study
Patients whose pelvic pain originates from other organs
Use of gonadotropins or other hormones three months before surgery

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain. Timepoint: Before surgery, 3 and 6 months after surgery. Method of measurement: Pelvic pain and dyspareunia scores are evaluated using the Visual Analogue Scale (VAS) and dysuria and dyschezia using a three-point score questionnire by possible answers to the items were yes”, no”, and a little”.
Secondary Outcome Measures
NameTimeMethod
Quality of life. Timepoint: Before surgery, 3 and 6 months after surgery. Method of measurement: Quality of life was measured using WHOQOL-BREF.;Edverse effects of the treatment. Timepoint: 3 and 6 months after surgery. Method of measurement: Questionnaire.;Pain recurrence. Timepoint: 6 months after surgery. Method of measurement: Questionnaire.
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