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the Value of Immunohistochemical Expression of Moesin in Endometrial Hyperplasia and Endometrial Carcinoma

the Value of Immunohistochemical Expression of Moesin in Endometrial Hyperplasia and Endometrial Carcinoma

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05619159
Enrollment
100
Registered
2022-11-16
Start date
2022-11-30
Completion date
2023-05-31
Last updated
2022-11-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Endometrial Cancer and Endometrial Hyperplasia

Brief summary

Endometrial carcinoma (EC) is the most prevalent invasive carcinoma of the female genital tract in developed countries, while it ranks as the second most frequently occurring neoplasm of women in developing countries, after carcinoma of the cervix uteri. The vast majority of ECs occur in perimenopausal and postmenopausal women . ECs are classified into two distinct phenotypes; type I which represents more than 80% of all cases of ECs, it has a favorable prognosis. This type is linked to excess, unopposed hyper-estrogenic condition and it is almost always preceded by endometrial hyperplasia. On the contrary, type II endometrial carcinoma is less common than type I, representing less than 10% of all cases of ECs. Type II endometrial carcinomas are high grade, poorly differentiated and estrogen-independent tumors .

Interventions

DEVICEmicroscopic pathological evaluation

description of moesin expression between endometrial hyperplasia and endometrial carcinoma

Sponsors

Sohag University
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
FEMALE

Inclusion criteria

* Hysterectomy specimens diagnosed as endometrial hyperplasia and endometrial adenocarcinoma. * All cases of endometrial biopsies obtained by curettage (D&C) diagnosed as endometrial hyperplasia. * Cases of cyclical endometrium obtained from endometrial curettage or hysterectomy specimens done for pathological conditions other than hyperplastic or neoplastic endometrial lesions. * Complete clinical data.

Exclusion criteria

* Patients with a history of preoperative chemotherapy and /or radiotherapy. * Biopsies with predominantly blood clots. * Insufficient or tiny tissue biopsies.

Design outcomes

Primary

MeasureTime frameDescription
The value of immunohistochemical expression of moesin in endometrial hyperplasia and endometrial carcinoma1 yearTo evaluate immunohistochemical expression of moesin in normal, hyperplasic and neoplastic endometrial tissues , correlate this expression with different clinicopathologic parameters of endometrial carcinoma and to evaluate the role of moesin as prognostic marker in progression from preinvasive lesions of the endometrium to endometrial carcinoma.

Countries

Egypt

Contacts

Primary Contactnermine a abd el fattah, resident doctor
nermine_abbas_post@med.sohag.edu.eg01018254748
Backup Contactafaf t el nashar, professor

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026