Viewing Study NCT04685460



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Last Modification Date: 2024-10-26 @ 1:52 PM
Study NCT ID: NCT04685460
Status: UNKNOWN
Last Update Posted: 2021-04-19
First Post: 2020-11-18

Brief Title: 3D Printed Bolus in Post-mastectomy Radiotherapy
Sponsor: Jiangxi Provincial Cancer Hospital
Organization: Jiangxi Provincial Cancer Hospital

Study Overview

Official Title: Clinical Study of 3D Printed Bolus for Volumetric Modulated Arc Therapy of Post-mastectomy Treatment
Status: UNKNOWN
Status Verified Date: 2020-11
Last Known Status: RECRUITING
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: Recently there is growing interest in the application of three-dimensional 3D printed bolus to radiotherapyAt present the researches on the application of 3D-printed bolus in breast cancer are mainly focused on air gap between skin and bolus or electron beam conformal therapy 715 there are no clinical experience with customized 3D-printed bolus for volumetric modulated arc therapy VMAT in daily practice has been published up to now We aim to evaluate dosimetry and application of 3D-printed bolus for the post-mastectomy radiotherapy PMRT with Volumetric modulated arc therapy VMAT Seventy five patients with breast cancer receiving radiotherapy following post-mastectomy in our department were randomly selected in this study The accuracy of fit of the 3D-Printed bolus to the chest wall was improved significantly relative to conventional bolusThis study demonstrates customized 3D-printed bolus in post-mastectomy radiation therapy improves fit of the bolus compared to conventional bolus Furthermore VMAT based on 3D-printed bolus significantly improves the chest wall target coverage and the conformity of plan and reduces the dose of ipsilateral lung and heart compared to conventional bolus
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None