Endometriosis
Conditions
Brief summary
Primary aim of this study is to evaluate the change in systemic inflammation parameters after surgery for superficial, ovarian or deep endometriosis. Secondary objectives focus on correlating these parameters to clinical outcomes, in patients with pelvic pain, and reproductive outcomes, in women desiring offspring. Participants already scheduled for surgery as part of their endometriosis care will be followed regarding the abovementioned outcomes after calculation of pre and postsurgical systemic inflammation markers (neutrophil to lymphocyte ratio; platelet to lymphocyte ratio and lymphocyte to monocyte ratio)
Interventions
None listed
Sponsors
University of Campania Luigi Vanvitelli
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
FEMALE
Age
18 Years to 45 Years
Inclusion criteria
* Age between 18 and 45 years. * Postoperative follow-up of at least 12 months; * Signature of informed consent regarding laparoscopic surgical treatment. * Signature of informed consent to the processing of personal data duly documented by medical records.
Exclusion criteria
* Failure to sign informed consent for laparoscopic surgical treatment * Histologic diagnosis of borderline tumor and/or ovarian carcinoma and/or mucinous cystadenoma and/or germ cell tumor or other malignancy of the genital tract * postoperative follow-up of less than 12 months; * documented history of inflammatory, rheumatologic, or immunologic disease; and * failure to provide informed consent for personal data processing.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Neutrophil to lymphocyte ratio | Measured before and after (24 to 72 hours) surgery |
Secondary
| Measure | Time frame |
|---|---|
| Platelet to lymphocyte ratio | Measured before and after (24 to 72 hours) surgery |
| Lymphocyte to monocyte ratio | Measured before and after (24 to 72 hours) surgery |
Countries
Italy
Contacts
Primary ContactGaetano Riemma, MD
Outcome results
None listed