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Spots Global Cancer Trial Database for Pre-operative 3-DCRT vs IMRT for Locally Advanced Rectal Cancer

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Trial Identification

Brief Title: Pre-operative 3-DCRT vs IMRT for Locally Advanced Rectal Cancer

Official Title: Randomised Phase II Study of Pre-operative 3-D Conformal Radiotherapy (3-DCRT) Versus Intensity Modulated Radiotherapy (IMRT) for Locally Advanced Rectal Cancer

Study ID: NCT02151019

Interventions

IMRT

Study Description

Brief Summary: The study aims to compare the incidence of acute grade 2 GI toxicity in the Control 3-D Conformal Radiotherapy compared to the Intensity Modulated Radiotherapy (IMRT) arm for locally advanced rectal cancer.

Detailed Description: Pre-operative radiotherapy (RT) or chemo-radiotherapy (CRT) is internationally accepted as standard practice in the management of locally advanced rectal cancer. Multiple randomised trials have proved pre-operative CRT and RT, compared to surgery alone, reduce local recurrence, even prior to optimal surgery, and may improve survival for T3 circumferential resection margin (CRM) negative patients. This study aims to determine if 3-DCRT or IMRT result in lower incidence of grade 2 GI toxicities. Acute toxicities will be assessed weekly during radiotherapy, and at 2 and 4 week post treatment. Late toxicities will be assessed at 3, 6, 9, 12, 18, 24 months post treatment, and annually to 10 years.

Keywords

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

St Luke's Radiation Oncology Network at Beaumont Hospital, Dublin, , Ireland

St Luke's Centre for Radiation Oncology at St James Hospital, Dublin, , Ireland

St Luke's Centre for Radiation Oncology at St Lukes Hospital, Dublin, , Ireland

Contact Details

Name: Dr Brian O'Neill, MD

Affiliation: St Luke's Centre for Radiation Oncology

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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