NCT06707025

Brief Summary

The investigators found an inverse relationship between CD24 and MiR-122 levels. Then the investigators found that CD24 that goes up with MiR-122 down makes macrophages unable to engulf the tumor cells. All this in mice. the investigators are interested in confirming this result in humans. Details of the preliminary results are attached to the submission of the research documents. the investigators will compare Cholangiocarcinoma tumors with other solid tumors, including liver tissue. The need to deepen understanding the investigators will also make a comparison between cancerous tissue and "normal" tissue adjacent to the tumor.

Trial Health

75
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
50

participants targeted

Target at P25-P50 for all trials

Timeline
6mo left

Started Nov 2023

Typical duration for all trials

Geographic Reach
1 country

1 active site

Status
active not recruiting

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

Study Progress84%
Nov 2023Oct 2026

Study Start

First participant enrolled

November 10, 2023

Completed
12 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 1, 2024

Completed
9 days until next milestone

First Submitted

Initial submission to the registry

November 10, 2024

Completed
17 days until next milestone

First Posted

Study publicly available on registry

November 27, 2024

Completed
1.9 years until next milestone

Study Completion

Last participant's last visit for all outcomes

October 28, 2026

Expected
Last Updated

March 14, 2025

Status Verified

October 1, 2024

Enrollment Period

12 months

First QC Date

November 10, 2024

Last Update Submit

March 11, 2025

Conditions

Keywords

CD24HumanLiver cancerMiR122

Outcome Measures

Primary Outcomes (1)

  • the investigators will analyze ductular reaction and cancer stem cells markers including CD24, CD44

    the investigators will perform the analysis on tissue samples of cholangiocarcinoma and non tumor controls, using immunohistochemistry and RT-PCR

    All along the study, from the first recruitment to the last recruitment. average of 1 year

Eligibility Criteria

Age18 Years - 85 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Patients with liver cancer.

You may qualify if:

  • \* Donors with cholangiocarcinoma samples

You may not qualify if:

  • \* Donors who do not have cholangiocarcinoma samples

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Hdassah Hospital

Jerusalem, Israel, 9112001, Israel

Location

Biospecimen

Retention: SAMPLES WITH DNA

the investigators are collecting plasma circulating free DNA. the investigators are not performing DNA sequencing. this is similar to chipSEQ.

MeSH Terms

Conditions

CholangiocarcinomaLiver Neoplasms

Condition Hierarchy (Ancestors)

AdenocarcinomaCarcinomaNeoplasms, Glandular and EpithelialNeoplasms by Histologic TypeNeoplasmsDigestive System NeoplasmsNeoplasms by SiteDigestive System DiseasesLiver Diseases

Study Officials

  • Tamar Hamburger

    Hadassah Hospital Hebrew University

    STUDY CHAIR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

November 10, 2024

First Posted

November 27, 2024

Study Start

November 10, 2023

Primary Completion

November 1, 2024

Study Completion (Estimated)

October 28, 2026

Last Updated

March 14, 2025

Record last verified: 2024-10

Data Sharing

IPD Sharing
Will share

Publication

Shared Documents
STUDY PROTOCOL, SAP, ICF, CSR, ANALYTIC CODE
Time Frame
January 2028 for 7 years
Access Criteria
After publication any one.
More information

Locations