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Evaluate the Effectiveness and Toxicity of Adjuvant Ultra-hypofractionated Radiotherapy for Breast Cancer - Trial NCT05850637

Access comprehensive clinical trial information for NCT05850637 through Pure Global AI's free database. This Phase 2 trial is sponsored by Prevent Senior Institute and is currently Completed. The study focuses on Breast Cancer Female. Target enrollment is 60 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.

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NCT05850637
Phase 2
Completed
radiation
Trial Details
ClinicalTrials.gov โ€ข NCT05850637
View on ClinicalTrials.gov
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Evaluate the Effectiveness and Toxicity of Adjuvant Ultra-hypofractionated Radiotherapy for Breast Cancer
Phase II Study to Evaluate the Effectiveness and Toxicity of Adjuvant Ultra-hypofractionated Radiotherapy for the Treatment of Early and Locally Advanced Breast Cancer

Study Focus

Breast Cancer Female

adjuvant ultra-hypofractionated radiotherapy

Interventional

radiation

Sponsor & Location

Prevent Senior Institute

Sรฃo Paulo, Brazil

Timeline & Enrollment

Phase 2

Jan 30, 2019

Apr 01, 2023

60 participants

Primary Outcome

Acute toxicity,Late toxicity

Summary

Prospective phase 2 study to evaluate the safety and efficacy of ultra-hypofractionated
 adjuvant radiotherapy in 5 fractions of 5.7 Gy in patients aged over 65 years.

ICD-10 Classifications

Malignant neoplasm: Breast, unspecified
Malignant neoplasm of breast
Malignant neoplasm of breast
Carcinoma in situ of breast, unspecified
Personal history of malignant neoplasm of breast

Data Source

ClinicalTrials.gov

NCT05850637

Non-Device Trial