- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07413263
Impact of Tyrosine Kinase Inhibitors on Glucose Level and Lipid Metabolism in Chronic Myeloid Leukemia Patients
February 14, 2026 updated by: Nancy Atef Abdou Mousa, Assiut University
Impact of Tyrosine Kinase Inhibitors on Glucose and Lipid Metabolism in Chronic Myeloid Leukemia
to known the impact of drugs that used in CML pt as TKIs on glucose and lipid metabolism
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Detailed Description
to known the impact of drugs that used in CML pt as TKIs on glucose and lipid metabolism and how danger they drugs be
Study Type
Observational
Enrollment (Estimated)
75
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: Nancy Atef Abdou, doctor
- Phone Number: 01153253658 01027607363
- Email: nancyatef918@gamil.com
Study Contact Backup
- Name: mai mostafa kamal, prof
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
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Sampling Method
Non-Probability Sample
Study Population
CML patients
Description
Inclusion Criteria:
- CML patients free medical history
Exclusion Criteria:
- diabetic
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in HbA1c levels in patients with chronic myeloid leukemia treated with tyrosine kinase inhibitors
Time Frame: Baseline and 3, 6, 9, and 12 months
|
Assessment of change in HbA1c levels in CML patients treated with TKIs.
|
Baseline and 3, 6, 9, and 12 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in lipid profile in patients with chronic myeloid leukemia treated with tyrosine kinase inhibitors
Time Frame: Baseline and 3, 6, 9, and 12 months
|
Assessment of changes in lipid profile including total cholesterol, triglycerides, LDL, and HDL in CML patients treated with TKIs.
|
Baseline and 3, 6, 9, and 12 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Mona mohamed soliman, prof, 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 (Estimated)
May 1, 2026
Primary Completion (Estimated)
December 30, 2027
Study Completion (Estimated)
December 30, 2028
Study Registration Dates
First Submitted
November 27, 2025
First Submitted That Met QC Criteria
February 9, 2026
First Posted (Actual)
February 17, 2026
Study Record Updates
Last Update Posted (Actual)
February 18, 2026
Last Update Submitted That Met QC Criteria
February 14, 2026
Last Verified
November 1, 2025
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Pathologic Processes
- Neoplasms
- Chronic Disease
- Disease Attributes
- Neoplasms by Histologic Type
- Hematologic Diseases
- Leukemia, Myeloid
- Bone Marrow Diseases
- Leukemia
- Myeloproliferative Disorders
- Pathological Conditions, Signs and Symptoms
- Hemic and Lymphatic Diseases
- Leukemia, Myelogenous, Chronic, BCR-ABL Positive
- Molecular Mechanisms of Pharmacological Action
- Enzyme Inhibitors
- Protein Kinase Inhibitors
- Organic Chemicals
- Heterocyclic Compounds, 1-Ring
- Heterocyclic Compounds
- Pharmacologic Actions
- Chemical Actions and Uses
- Hydrocarbons
- Hydrocarbons, Cyclic
- Carboxylic Acids
- Hydrocarbons, Aromatic
- Amides
- Pyrimidines
- Benzene Derivatives
- Acids, Carbocyclic
- Benzoates
- Benzamides
- Piperazines
- Imatinib Mesylate
- Tyrosine Kinase Inhibitors
- nilotinib
Other Study ID Numbers
- use of TKIs on CML
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
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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