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临床试验/NCT07029373
NCT07029373已完成不适用

A Prospective Clinical Study for Analyzing Plasma Calcitonin Gene-Related Peptide (CGRP) Levels in Patients With Head and Neck Malignancies Undergoing Radiotherapy

West China Hospital1 个研究点 分布在 1 个国家目标入组 23 人开始时间: 2025年7月4日最近更新:

试验速览

阶段
不适用
状态
已完成
入组人数
23
试验地点
1
主要终点
Change in plasma CGRP level

研究概览

简要总结

This prospective study investigates the dynamic changes in plasma calcitonin gene-related peptide (CGRP) levels during radiotherapy and their association with radiotherapy-related pain in patients with head and neck malignancies.

详细描述

Radiotherapy-related pain is a major clinical challenge that significantly affects the long-term quality of life and treatment adherence of patients with head and neck cancer. Current analgesic strategies offer limited efficacy, and reliable biomarkers for predicting pain risk are lacking. In recent years, calcitonin gene-related peptide (CGRP) has drawn increasing attention for its critical role in chronic pain regulation, as demonstrated in various pain models. However, no systematic studies have yet investigated the expression patterns and clinical relevance of CGRP in radiotherapy-induced pain among patients with head and neck malignancies. This single-center, prospective observational study aims to enroll patients with head and neck cancer receiving either definitive or postoperative adjuvant radiotherapy. Plasma samples will be collected before, during, and after radiotherapy for measurement of CGRP levels. Pain intensity will be simultaneously assessed using the Numeric Rating Scale (NRS) and the Brief Pain Inventory-Short Form (BPI-SF). The study seeks to explore the dynamic changes in plasma CGRP levels throughout the radiotherapy course and to analyze their correlation with patient-reported pain, thereby providing potential insights into biomarker-based pain prediction and management strategies in this patient population.

研究设计

研究类型
Observational
观察模型
Other
时间视角
Prospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age ≥ 18 years
  • Histologically confirmed head and neck malignancy
  • Planned to receive definitive or postoperative adjuvant radiotherapy
  • Radiotherapy duration ≥ 4 weeks, with irradiation field involving the oral cavity, pharynx, or neck region
  • Able and willing to provide written informed consent
  • Able to complete pain assessments and blood sample collection

排除标准

  • History of significant chronic pain prior to radiotherapy (e.g., postherpetic neuralgia, rheumatoid arthritis)
  • Presence of uncontrolled hypertension, diabetes, or migraines
  • Presence of other active malignancies or major systemic diseases (e.g., severe hepatic or renal dysfunction)
  • Currently receiving or recently received treatments that may significantly affect pain perception (e.g., opioids, antidepressants)
  • Pregnant or breastfeeding
  • Inability to complete follow-up or poor treatment compliance

结局指标

主要结局

Change in plasma CGRP level

时间窗: Baseline (prior to the initiation of radiotherapy), At the end of the third week of radiotherapy (approximately 21±2 days after the 15th radiotherapy session), Within one week after the completion of radiotherapy.

To assess dynamic changes in CGRP levels during the course of radiotherapy.

Correlation between CGRP levels and pain scores (NRS and BPI-SF)

时间窗: Baseline (prior to the initiation of radiotherapy), At the end of the third week of radiotherapy (approximately 21±2 days after the 15th radiotherapy session), Within one week after the completion of radiotherapy.

To evaluate the association between CGRP expression and radiotherapy-induced pain.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Xingchen Peng

PhD, Professor

West China Hospital

研究点 (1)

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