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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04412902
Other study ID # 109053-E
Secondary ID
Status Completed
Phase
First received
Last updated
Start date April 25, 2020
Est. completion date November 25, 2020

Study information

Verified date April 2020
Source Far Eastern Memorial Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study will analyze whether there is any difference in recurrence and survival rates among the patients who received different adjuvant therapies.


Description:

The incidence of endometrial cancer is gradually increasing nowaday. The postoperative treatment of high-risk endometrial cancer is also inconsistent. Besides, the recurrence of high-risk endometrial cancer is high.The investigators retrospective study will analyze the factors associated with recurrence of endometrial cancer, especially for different adjuvant therapies.


Recruitment information / eligibility

Status Completed
Enrollment 92
Est. completion date November 25, 2020
Est. primary completion date October 25, 2020
Accepts healthy volunteers No
Gender Female
Age group 20 Years and older
Eligibility Inclusion Criteria: - All patients with high risk stage I endometrial cancer and all patients with stage II and stage III endometrial cancer and who underwent therapy in Far Eastern Memorial Hospital from 2009/01/01~2019/09/17. Exclusion Criteria: - Patients with stage I endometrial cancer do not have high risk factors.

Study Design


Intervention

Drug:
adjuvant therapy
Adjuvant chemotherapy and/or radiotherapy

Locations

Country Name City State
Taiwan Department of Obstetrics and Gynecology, Far-Eastern Memorial Hospital Banqiao New Taipei

Sponsors (1)

Lead Sponsor Collaborator
Far Eastern Memorial Hospital

Country where clinical trial is conducted

Taiwan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Factors affecting overall survival Factors affecting overall survival 10 years
Secondary Factors affecting progression-free survival Factors affecting progression-free survival 10 years