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Combined drug-surgical technique for the treatment of endometriosis

Not Applicable
Conditions
Endometriosis.
Endometriosis
Registration Number
IRCT20190714044201N2
Lead Sponsor
Sarem Fertility and Infertility Research Center
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
20
Inclusion Criteria

Laparoscopy with the initial diagnosis and confirmation of endometriosis stages
Informed consent form for inclusion

Exclusion Criteria

People with confirmed severe adenomyosis with advanced endometriosis
People with endometrial lesions on the pelvic nerves
People who have previously undergone endometrial surgery.
People who have recently (less than 6 months) received GnRH agonist.

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pelvic pain. Timepoint: Before the intervention and six months after the intervention. Method of measurement: Vaginal analogous scale.;Pain during menstruation. Timepoint: Before the intervention and six months after the intervention. Method of measurement: Vaginal analogous scale.
Secondary Outcome Measures
NameTimeMethod
Recurrence of Endometriosis. Timepoint: Six months and one year after the intervention. Method of measurement: Clinical assessment.
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