- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05690399
Evaluation of Clinical and Pathological Characteristics and Routine Treatment of Patients With Prostate Cancer
January 10, 2023 updated by: Aml Mohamed Haridy, Assiut University
Evaluation of Clinical and Pathological Characteristics and Routine Treatment of Patients With Prostate Cancer in 2 Centers in Asyut
To evaluate clinical and pathological characteristics and treatment protocol and outcomes of patients with prostate cancer in 2 centers of Asyut from 2013 to 2023
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Detailed Description
Inclusion criteria :
- Male patient , Age ≥ 40 yo
- Diagnosed as prostate cancer from ( 2013- 2023 ) proved by biopsy in South Egypt Cancer Institute "SECI" & Asyut clinical oncology department
- Newly diagnosed/ metastatic at presentation
ECOG 0-4
• Exclusion criteria:
- Having Other types of malignancy.
Study Type
Observational
Enrollment (Anticipated)
100
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Aml Haridy
- Phone Number: 01061119919
- Email: Amlmohamed1195@gmail.com
Study Contact Backup
- Name: Heba Bakry
- Phone Number: 01007272760
- Email: heba_bakri@aun.edu.eg
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
40 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
N/A
Genders Eligible for Study
Male
Sampling Method
Non-Probability Sample
Study Population
Diagnosed as prostate cancer from ( 2013- 2023 ) proved by biopsy
- Newly diagnosed/ metastatic at presentation
Description
Inclusion Criteria:
- Male patient , Age ≥ 40 yo
- Diagnosed as prostate cancer from ( 2013- 2023 ) proved by biopsy
- Newly diagnosed/ metastatic at presentation
- ECOG 0-4
Exclusion Criteria:
- Having Other types of malignancy.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Case-Control
- Time Perspectives: Retrospective
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Clinical and pathological characteristics and routine treatment of patients with prostate cancer in 2 centers in Asyut in previous 10 years
Time Frame: Baseline
|
Clinical and pathological characteristics and routine treatment of patients with prostate cancer in 2 centers in Asyut in previous 10 years
|
Baseline
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: assiut university, Assiut University
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Anticipated)
January 1, 2023
Primary Completion (Anticipated)
March 1, 2024
Study Completion (Anticipated)
April 1, 2024
Study Registration Dates
First Submitted
January 10, 2023
First Submitted That Met QC Criteria
January 10, 2023
First Posted (Actual)
January 19, 2023
Study Record Updates
Last Update Posted (Actual)
January 19, 2023
Last Update Submitted That Met QC Criteria
January 10, 2023
Last Verified
January 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Prostate cancer
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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