Frequency of Pulmonary Toxicity in Patients Treated for Hodgkin Lymphoma
1 other identifier
observational
214
1 country
1
Brief Summary
Pulmonary toxicity during Hodgkin lymphoma treatment is significant for a variety of reasons, ranging from clinical care to therapeutic innovation and patient outcomes.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Feb 2024
1 active site
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
Study Start
First participant enrolled
February 18, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 15, 2024
CompletedFirst Submitted
Initial submission to the registry
December 19, 2024
CompletedFirst Posted
Study publicly available on registry
January 7, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
March 1, 2025
CompletedJanuary 7, 2025
January 1, 2025
5 months
December 19, 2024
January 5, 2025
Conditions
Outcome Measures
Primary Outcomes (1)
high-resolution computed tomography
An HRCT (high-resolution computed tomography) scan is a type of CT scan healthcare providers use to get detailed images of your lungs. Providers most commonly use it to diagnose and monitor interstitial lung diseases and conditions that affect your small airways and alveoli (air sacs).
12 Months
Interventions
To determine treatment-induced pulmonary toxicity prevalence and risk factors in Hodgkin lymphoma patients during chemotherapy or radiation therapy.
Eligibility Criteria
to check the Frequency of Pulmonary Toxicity in Patients Treated for Hodgkin Lymphoma
You may qualify if:
- Patients diagnosed with Hodgkin lymphoma (HL) receiving treatment.
- Patients of all ages and both genders.
- Patients with histologically confirmed HL, as per the WHO 2016 classification.
- Patients who have undergone pulmonary function testing and assessment at specified time points during their treatment course.
- Patients with complete medical records documenting treatment regimens, including chemotherapy and radiotherapy details.
You may not qualify if:
- Patients with a diagnosis of another malignancy.
- Patients with incomplete medical records or missing data on treatment regimens and pulmonary function assessments.
- Patients with a history of significant pulmonary comorbidities, such as chronic obstructive pulmonary disease (COPD), interstitial lung disease, or pulmonary fibrosis, before HL diagnosis.
- Patients who are unable to complete pulmonary function tests.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Shaukat Khanum Memorial Cancer Hospital and Research Centre, 5-B, Sector A2, Phase 5, Hayatabad
Peshawar, Khyber Pakhtunkhwa, Pakistan
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- CASE CONTROL
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
December 19, 2024
First Posted
January 7, 2025
Study Start
February 18, 2024
Primary Completion
July 15, 2024
Study Completion
March 1, 2025
Last Updated
January 7, 2025
Record last verified: 2025-01
Data Sharing
- IPD Sharing
- Will not share