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A STUDY TO COMPARE THE EFFICACY OF THREE DIFFERENT DOSE FRACTIONATION REGIMENS IN PALLIATIVE RADIOTHERAPY FOR PATIENTS WITH PAINFUL BONE METASTASIS A study to compare the efficacy of three different dose fractionation regimens in palliative radiotherapy for patients with painful bone metastasis.

A prospective randomized study to compare the efficacy of three different dose fractionation regimens in palliative radiotherapy for patients with painful bone metastasis. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/08/072254
Enrollment
195
Registered
2024-08-09
Start date
Unknown
Completion date
Unknown
Last updated
2024-08-19

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

Conditions

Health Condition 1: C795- Secondary malignant neoplasm of bone and bone marrow

Interventions

Intervention1: Radiation therapy to bone metastasis using 3 different treatment schedules: Dose of 8Gy in 1 fraction, Dose of 20 Gy in 5 fractions, Dose of 30 Gy in 10 fractions Control Intervention1

Sponsors

Sri Venkateshwara Institute of medical sciences
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Radiologically evident bone metastases from any primary tumor site. 2.Patients with pain due to bone metastasis 3.Patients with uncomplicated bone pain 4.ECOG performance status 0-3 5.Patients who have given informed consent 6.Patients of age 18yrs or older

Exclusion criteria

Exclusion criteria: 1.Previous history of radioisotope treatment 2.Previous surgical intervention to same location 3.Patients with pathological fracture 4.Pregnant and lactating women

Design outcomes

Primary

MeasureTime frame
Pain score assessment will be done among patients receiving 3 different treatment schedules during the course of treatment, at 1 month ,2 months and 3 months of follow upTimepoint: 1 month, 2 months, 3 months

Secondary

MeasureTime frame
1.To determine the analgesic requirement by using narcotic score . 2.To determine the improvement in performance status by using ECOG 3.To determine improvement in quality of life by using BOMET-QOL questionnaireTimepoint: every month for 3 months after completion of treatment

Countries

India

Contacts

Public ContactG Sindhu

Sri venkateswara institute of medical sciences tirupati

daspranabandhu@gmail.com9493547731

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026