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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT03464799
Other study ID # KanuniSSRTH
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date September 2018
Est. completion date December 2018

Study information

Verified date August 2018
Source Kanuni Sultan Suleyman Training and Research Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Pathological specimens of 40 women that had been operated for endometriosis will be included in this study. These tissues will be stained with a marker named as PDL-1 in pathological examination. "programmed cell death (PD-1)" is expressed on T cells. The immunotherapies in which antibodies against these PD-1 and its ligands (PDL-1) have been used are accepted as very effective in the treatment of many cancers. If these ligands can be shown in the endometriosis, it will be an important step for the treatment of endometriosis.


Description:

40 women who had been operated for endometriosis between 2013 and 2014 will be included in this study. Pathological specimens will be stained with an immunohistochemical marker named as PDL-1. "programmed cell death (PD-1)" is a protein containing 288 aminoacids and expressed on T cells. It was shown on apoptotic cells in earlier times, but then it has been understood that its physiologic role is not cell death. The upregulation of PD-1 is a result of the activation of T cells and it is necessary for the termination of immune response. PD-L1 is a ligand for PD-1. The immunotherapies in which antibodies against these PD-1 and its ligands (especially PDL-1) provides significant improvements in many cancers such as melanoma. Evidence about the role of these ligands in endometriosis will be an important step in its management.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 40
Est. completion date December 2018
Est. primary completion date December 2018
Accepts healthy volunteers No
Gender Female
Age group N/A and older
Eligibility Inclusion Criteria:

- patients operated for endometriosis between 2013 and 2014

- pathological examinations proving the diagnosis of endometriosis

Exclusion Criteria:

- patients operated for cysts other than endometriosis

Study Design


Related Conditions & MeSH terms


Intervention

Other:
immunohistochemical staining
immunohistochemical staining

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Kanuni Sultan Suleyman Training and Research Hospital

Outcome

Type Measure Description Time frame Safety issue
Primary immunohistochemical staining immunohistochemical staining with PD-L1 6 months
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