Viewing Study NCT06630780



Ignite Creation Date: 2024-10-26 @ 3:42 PM
Last Modification Date: 2024-10-26 @ 3:42 PM
Study NCT ID: NCT06630780
Status: NOT_YET_RECRUITING
Last Update Posted: None
First Post: 2024-09-17

Brief Title: Reduction of Postoperative Radiotherapy in Head and Neck Squamous Cell Carcinoma
Sponsor: None
Organization: None

Study Overview

Official Title: A Prospective Phase II Clinical Trial on the Reduction of Postoperative Radiotherapy in Head and Neck Squamous Cell Carcinoma
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: REPORT-HNSCC
Brief Summary: To explore the control rate and quality of life of participants with late head and neck squamous cell carcinoma who have obtained postoperative pCR after cervical lymph node surgery with neoadjuvant chemotherapy combined with immunotherapy and the cervical lymph node removal prophylactic irradiation ENI in the low-risk area
Detailed Description: In order to understand whether it can better protect normal tissues such as pharyngeal constriction muscles thyroid parotid glands and submandibular glands without affecting the efficacy of tumors and reduce the negative impact of radiotherapy on immunotherapy the investigators plan to conduct a prospective phase II study to explore the control rate and quality of life of patients with late head and neck squamous cell carcinoma who have obtained postoperative pCR after cervical lymph node surgery with neoadjuvant chemotherapy combined with immunotherapy

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