Superficial and Deep Endometriosis: Role of Systemic Inflammation as a Marker of Clinical, Surgical, and Reproductive Outcomes

Status: Recruiting
Location: See location...
Study Type: Observational
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)

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 18
Maximum Age: 45
View:

• 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.

Locations
Other Locations
Italy
University of Campania Luigi Vanvitelli
RECRUITING
Napoli
Contact Information
Primary
Gaetano Riemma, MD
gaetano.riemma@unicampania.it
0038 0815665599
Time Frame
Start Date: 2024-05-29
Estimated Completion Date: 2026-06
Participants
Target number of participants: 138
Treatments
Superficial Endometriosis
Laparoscopic excision of superficial (peritoneal) endometriotic implants
Ovarian Endometriosis
Laparoscopic excision of ovarian endometrioma/s
Deep Infiltrating Endometriosis (DIE)
Laparoscopic excision of DIE
Related Therapeutic Areas
Sponsors
Leads: University of Campania Luigi Vanvitelli

This content was sourced from clinicaltrials.gov

Similar Clinical Trials