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Dexamethasone for the Prophylaxis of Pain Flare Study

Dexamethasone for the Prophylaxis of Radiation-Induced Pain Flare Following Palliative Radiotherapy for Bone Metastases

Status
Completed
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00438828
Enrollment
61
Registered
2007-02-22
Start date
2007-02-28
Completion date
2011-07-31
Last updated
2014-11-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cancer

Keywords

radiation therapy, palliative, pain

Brief summary

Radiation treatment is often recommended as a safe and quick treatment that gives most people good relief from bone pain within a couple of weeks. However, some people can experience a short episode of increased pain (called a 'flare') a day or two after radiation treatment, that lasts about a day. The purpose of this sturdy is to find out if a medication called dexamethasone can help prevent pain flare as a result of radiation therapy.

Detailed description

Of all people diagnosed with cancer, 25% will have their cancer come back and spread to the bones. This often results in significant pain and suffering. Radiation treatment is often recommended as a safe and quick treatment that gives most people good relief from bone pain within a couple of weeks. However, some people can experience a short episode of increased pain called a flare a day or two after radiation treatment that lasts about a day. Studies suggest that around a third of all people who receive radiation treatment to help pain from cancer in the bones will have a pain flare. This study is being done because it would be helpful to prevent extra bone pain from happening to people after they receive radiation treatments. The purpose of this study is to find out if a medication called dexamethasone can help prevent pain flare as a result of radiation therapy.

Interventions

DRUGdexamethasone

8mg Dexamethasone PO on days 0 (prior to radiation treatment), and days 1, 2, and 3 following radiation treatment.

Sponsors

Sunnybrook Health Sciences Centre
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Documented bone metastases by radiological imaging * Patients at least 18 years of age * Written consent * KPS ≥ 40 * Baseline worst pain at the planned radiated bony metastatic site ≥ 2 * Patient able to inform the pain score at the planned radiated bony metastatic site

Exclusion criteria

* Concurrent use of any corticosteroid medication other than topical or inhaled preparations * Medical contraindications to corticosteroids such as diabetes mellitus, uncontrolled hypertension or active peptic ulcer * Pathological fracture of the irradiated extremity * Spinal cord compression * Language barrier * Immediate change in regular analgesic medication. If the oncologist thinks the patient is not receiving adequate analgesic, we recommend the oncologist to increase the analgesic first to stabilize ot lessen the pain before recruiting the patient to this study

Design outcomes

Primary

MeasureTime frame
Complete control of pain flare on days 1-5 after the completion of radiation treatment.Days 1-5

Secondary

MeasureTime frame
Complete control of pain flare from Day 6-10 after the completion of radiation treatment.Days 6-10
Functional interference especially mood and sleep in Brief Pain Inventory will be monitored.Days 0, 1-10, and 6-weeks from baseline assessment
Quality of life outcomesBaseline and 6-weeks following treatment

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026