Elastography and Treatment of Lymphoma
The Role of Sonoelastography in Evaluation of Therapeutic Response in Patients With Lymphoma.
1 other identifier
observational
44
0 countries
N/A
Brief Summary
To determine accuracy of elastography in assessment of superficial lymph nodes response to treatment in cases of lymphoma.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started Aug 2023
Typical duration for all trials
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
July 23, 2023
CompletedFirst Posted
Study publicly available on registry
August 1, 2023
CompletedStudy Start
First participant enrolled
August 1, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
November 1, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2025
CompletedAugust 1, 2023
July 1, 2023
2.3 years
July 23, 2023
July 23, 2023
Conditions
Outcome Measures
Primary Outcomes (1)
To determine accuracy of elastography in assessment of superficial lymph nodes response to treatment in cases of lymphoma.
Sonoelastography is a new technique that depends on the elastic properties of soft tissues, with the idea of malignant lesions being stiffer than benign or normal tissue. It may have a dependable role in evaluation of therapeutic response in patients with lymphoma and can be used for follow up, the same way it has been used in different parts of the body, such as the breast, and thyroid. To the best of our knowledge, there are few studies concerning the role of elastography in the field of lymphoma disease.
Average three years
Eligibility Criteria
Patients diagnosed as lymphoma , have superficial lymph nodes and not received any treatment
You may qualify if:
- patients who are histopathologically proven as lymphoma, not receive treatment and have superficial lymphadenopathy.
You may not qualify if:
- Lymphoma without superficial lymph nodes. 2-patients under treatment.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Kerols Refaat, Resident
Assiut University
- STUDY DIRECTOR
Nagham Nabil, Professor
Assiut University
- STUDY DIRECTOR
Abdel-Monem Sayed, Lecture
Assiut University
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Resident doctor
Study Record Dates
First Submitted
July 23, 2023
First Posted
August 1, 2023
Study Start
August 1, 2023
Primary Completion
November 1, 2025
Study Completion
December 1, 2025
Last Updated
August 1, 2023
Record last verified: 2023-07