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Hypofractionated radiotherapy boost in prostate cancer

LOCALIZED CARCINOMA PROSTATE: INTENSITY MODULATED RADIOTHERAPY (IMRT) FOLLOWED BY STEREOTACTIC BODY RADIOTHERAPY (SBRT) BOOST: A FEASIBILITY STUDY FOR ACUTE TOXICITY.

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2018/07/014948
Enrollment
15
Registered
2018-07-18
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: null- Prostate cancer

Interventions

Intervention1: INTENSITY MODULATED RADIOTHERAPY (IMRT) FOLLOWED BY STEREOTACTIC BODY RADIOTHERAPY (SBRT) BOOST: single arm of 15 patients of localised carcinoma prostate are treated with radiotherapy

Sponsors

Department of radiotherapy
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Previously untreated biopsy proven prostate adenocarcinoma. 2. Localized carcinoma prostate (Stage T1 T2 T3) as per TNM staging system. 3. Karnofsky performance scale (KPS) > 70 4. Normal Hemogram, renal and liver function. 5. Informed consent for participation in the study

Exclusion criteria

Exclusion criteria: 1. Carcinoma prostate other than adenocarcinoma histology. 2. Stage T4 3. Lymph nodal involvement N+ 4. Evidence of distant metastasis on chest X â?? ray or Bone Scan. 5. Patients having any uncontrolled co-morbid conditions. 6. Prior pelvic radiotherapy 7. Presence of 2nd malignancy

Design outcomes

Primary

MeasureTime frame
1. To assess the acute toxicity occurring with treatment with IMRT followed by SBRT boost in localized prostate cancerTimepoint: Toxicities are assessed -- a)weekly during radiotherapy treatment b)at the end of first,second and third months of radiotherapy completion

Secondary

MeasureTime frame
2. To evaluate the improvement or decline in urinary function with treatment. 3. To study the short-term treatment outcome on radiological basis. Timepoint: urinary function assesed weekly during treatment and 1st and 3rd month post treatment treatment response assessed post 3 months of treatment

Countries

India

Contacts

Public ContactDrNarendra kumar

PGIMER

drnarendra74@gmail.com9814968775

Outcome results

None listed

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