NCT06761599

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

55
Monitor

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
214

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Feb 2024

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 Start

First participant enrolled

February 18, 2024

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 15, 2024

Completed
5 months until next milestone

First Submitted

Initial submission to the registry

December 19, 2024

Completed
19 days until next milestone

First Posted

Study publicly available on registry

January 7, 2025

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

March 1, 2025

Completed
Last Updated

January 7, 2025

Status Verified

January 1, 2025

Enrollment Period

5 months

First QC Date

December 19, 2024

Last Update Submit

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

group 1DIAGNOSTIC_TEST

To determine treatment-induced pulmonary toxicity prevalence and risk factors in Hodgkin lymphoma patients during chemotherapy or radiation therapy.

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

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

Location

MeSH Terms

Conditions

Hodgkin Disease

Interventions

Chromosomes, Human, 1-3

Condition Hierarchy (Ancestors)

LymphomaNeoplasms by Histologic TypeNeoplasmsLymphoproliferative DisordersLymphatic DiseasesHemic and Lymphatic DiseasesImmunoproliferative DisordersImmune System Diseases

Intervention Hierarchy (Ancestors)

Chromosomes, HumanChromosomes, MammalianChromosomesGenetic StructuresGenetic Phenomena

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

Locations