laparoscopy of endometriosis. Endometriosis, unspecified
Conditions
Interventions
Intervention 1: Intervention group 1: group receiving dinogest 2mg/day continuously after surgery for 6 months. Intervention 2: Intervention group 2 : group receiving oral contraceptive (low dose mono
Sponsors
Esfahan University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
20 Years to 40 Years
Inclusion criteria
Inclusion criteria: Patients with diagnosis endometriosis via laparoscopy Premenopausal patients Patients who have symptoms of endometriosis before surgery (eg: dysmenorrhea, dyspareunia, chronic pelvic pain) Patients who have been referred to Isfahan's Alzhra and Shahid Beheshty hospitals Patients who do not have any decision for pregnancy during this study Patients with 20-40 years of age
Exclusion criteria
Exclusion criteria: Any hormonal therapy 3 months before surgery Having contraindications for using oral contraceptives Changing in the address so there is no access to the patient and her information History of surgery for treatment of endometriosis History of sexual dysfunction in patient or the partner Clients who undergo hysterectomy or ouophurectomy during surgery History of malignancy or heart disease
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Recurrence of endometriosis. Timepoint: 6 months. Method of measurement: visual analog scale, WHO quality of life brief (WHOQOL-BREF) , Female Sexual Function Index (FSFI).;Pain. Timepoint: 6 months. Method of measurement: visual analog scale, WHO quality of life brief ( WHOQOL-BREF), Female sexual function index (FSFI). | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactReihaneh Valian Broujeni
Esfahan University of Medical Sciences
Outcome results
None listed