Diffusion-weighted Magnetic Resonance Imaging in Post Therapy Patients With Lymphoma
1 other identifier
observational
50
0 countries
N/A
Brief Summary
- The goal of this study is to determine the feasibility of the diffusion weighted Magnetic Resonance Imaging in the evaluation of the treatment response in patients with malignant lymphoma.
- The investigator's objective is to compare the changes of mean Apparent Diffusion Coefficient value of the tumor with the changes of maximum Standardized Uptake Value of the tumor in positron Emission Tomography Computed Tomography in both pre and post therapy status .
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 Sep 2019
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
May 23, 2019
CompletedFirst Posted
Study publicly available on registry
May 31, 2019
CompletedStudy Start
First participant enrolled
September 1, 2019
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 30, 2021
CompletedStudy Completion
Last participant's last visit for all outcomes
January 30, 2022
CompletedMay 31, 2019
May 1, 2019
2.3 years
May 23, 2019
May 30, 2019
Conditions
Outcome Measures
Primary Outcomes (1)
role of diffusion weighted imaging in followup of lymphoma
• measures mean Apparent diffusion coefficient value in pre and post therapy status in patients with lymphoma with cut off value 1 .
5 minutes
Study Arms (1)
1 lymphoma patients
pre therapy and post therapy of lymphoma patients
Interventions
compare between result of positron emission tomography /computed tomography and diffusion weighted imaging in followup of lymphoma
Eligibility Criteria
patients diagnosed as malignant lymphoma
You may qualify if:
- patients clinically diagnosed as lymphoma patient can tolerate the magnetic resonance examination.
You may not qualify if:
- presence of paramagnetic substance as peace maker or cochlear implants and claustrophobia.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
sara, Msc
Assiut University
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- CASE CROSSOVER
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- principel investigator
Study Record Dates
First Submitted
May 23, 2019
First Posted
May 31, 2019
Study Start
September 1, 2019
Primary Completion
December 30, 2021
Study Completion
January 30, 2022
Last Updated
May 31, 2019
Record last verified: 2019-05