NCT06286371Completed
Pelvic Neuro-Angiogenesis in Deep Endometriosis
Pelvic Neuro-Angiogenesis Density in the Presence of Deep Endometriosis and Relationship Between Pelvic Pain Scores
Source: ClinicalTrials.gov · Last updated 29 Jan 2026
Brief summary (registry, in English)
Endometriosis is observed in one out of every ten women in society, causing endometrial cells to be found outside their normal location in the body and proliferate in other locations, leading to fibrosis in the tissue due to the secretion of various factors from the cells. Additionally, the substances secreted by the cells can cause various other changes in the tissue besides fibrosis. Increased neurogenesis and neovascularization are among the primary changes, which occur as a result of the secretion of substances from the cells. Increased neovascularization, neurogenesis, and fibrosis in the tissue lead to the formation of nodular structures in the pelvic region, resulting in pain development in women. Nodular formations in the pelvic region due to endometriosis are especially observed in the rectovaginal space. Despite being small in size, they can induce increased neovascularization and neurogenesis even in healthy peritoneal tissue due to the microenvironment they create, leading to different clinical symptoms clinically. However, it is not known how far these changes occur around the endometriotic nodule in the presence of endometriosis. In this project, in patients operated on due to endometriosis, the density of nerve and vascular structures in the surgical margins of the peritoneal tissue excised along with the nodule, and the synthesis and release of chemical mediators causing pain (e.g., Bradykinin, Substance-P) are evaluated. The aim is to determine the minimum surgical margin where excision should be applied in surgery and to demonstrate any endometriotic changes that may exist in the tissues, even though they may appear macroscopically healthy.
- Status (registry)
- Completed
- Study type
- Interventional
- Enrollment
- 15 (actual)
- First submitted
- 22 Feb 2024
- Start date
- 1 Dec 2023
- Primary completion date
- 23 Apr 2025
- Lead sponsor
- Uludag University
- Diseases
- Endometriosis
- NCT number
- NCT06286371
What you commit to
- Study type: Interventional
- Participants enrolled: 15
- From 1 Dec 2023 to the primary completion date, 23 Apr 2025
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Patients with extensive surgery (hysterectomy, ovariectomy)
- Patients with previous endometriosis or another pelvic surgery
Other illness
- Patients with pelvic inflammatory disease history
Other
- Patients with malignity suspicion
- Patients with oocyte pick up procedure history
Who the study is looking for
- Patients with suspicion of deep endometriosis (Physical Examination and MRI)
- Patients with ineffective response to medical therapy
- Patients who undergo laparoscopic conservative endometriosis surgery (douglasectomy)
Age in the registry: 18 years to 45 years · Sex: Female · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Uludag University Faculty Hospital Coordinator of this site? Confirm its status | Bursa | Turkey (Türkiye) | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.