Pretreatment Lymphocyte Monocyte Ratio on Outcome HCC Patients
The Impact of Pretreatment Lymphocyte to Monocyte Ratio on Clinical Outcome for Patient With HCC
1 other identifier
observational
1
0 countries
N/A
Brief Summary
To assess the prognostic role of pretreatment LMR in hepatocellular carcinoma(HCC).
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for all trials
Started Apr 2019
Shorter than P25 for all trials
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
March 7, 2019
CompletedFirst Posted
Study publicly available on registry
March 11, 2019
CompletedStudy Start
First participant enrolled
April 5, 2019
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 5, 2020
CompletedStudy Completion
Last participant's last visit for all outcomes
March 31, 2020
CompletedApril 2, 2019
March 1, 2019
11 months
March 7, 2019
March 31, 2019
Conditions
Outcome Measures
Primary Outcomes (1)
increased over all survival
Elevated pretreatment lymphocyte monocyte ratio may be a favorable prognostic factor for clinical outcomes in patients with hepatocellular carcinoma.
1 year
Interventions
lymphocyte and monocyte count
Eligibility Criteria
Hepatocellular carcinoma patients
You may qualify if:
- Patients with child A Hepatocellular carcinoma.
You may not qualify if:
- Patients with child C Hepatocellular carcinoma.
- Patients with heart failure
Contact the study team to confirm eligibility.
Sponsors & Collaborators
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY CHAIR
taha mahran, MD
Assiut University
- STUDY CHAIR
ola abdelfatah, MD
Assiut University
- STUDY DIRECTOR
aml ebraheem, MD
Assiut University
- PRINCIPAL INVESTIGATOR
amany amin, master
Assiut University
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Target Duration
- 1 Year
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
March 7, 2019
First Posted
March 11, 2019
Study Start
April 5, 2019
Primary Completion
March 5, 2020
Study Completion
March 31, 2020
Last Updated
April 2, 2019
Record last verified: 2019-03