Viewing Study NCT06641635



Ignite Creation Date: 2024-10-26 @ 3:42 PM
Last Modification Date: 2024-10-26 @ 3:42 PM
Study NCT ID: NCT06641635
Status: NOT_YET_RECRUITING
Last Update Posted: None
First Post: 2024-10-08

Brief Title: Moderated Hypofractionated Online Adaptive Radiotherapy in Cervical Cancer
Sponsor: None
Organization: None

Study Overview

Official Title: A Multicenter Non-inferiority Phase 3 Randomized Controlled Study of Moderated Hypofractionated Online Adaptive Radiotherapy for Cervical Cancer
Status: NOT_YET_RECRUITING
Status Verified Date: 2024-10
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The most common external beam radiotherapy fractionation scheme for cervical cancer is 45-504 Gy delivered in 25-28 fractions However prolonged treatment duration can lead to insufficient availability of medical resources We hope to assess the safety and efficacy of moderated hypofractionated online adaptive radiotherapy in combination with brachytherapy in patients with cervical cancer in a multicenter study
Detailed Description: This is a multicenter non-inferiority phase 3 randomized controlled study This study investigates the role of moderated hypofractionated online adaptive radiotherapy by randomizing patients to this experimental regimen versus the standard of treatmentThe purpose of this study is to access safety and efficacy of moderated hypofractionated online adaptive radiotherapy in combination with high-dose-rate brachytherapy in patients with cervical cancer which based on the previous research NCT05994300

Study Oversight

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