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临床试验/NCT07755176
NCT07755176Enrolling By Invitation不适用

Patient-reported Outcomes Following Percutaneous Ablation of Desmoid Tumors

Mayo Clinic1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2026年9月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
Enrolling By Invitation
发起方
Mayo Clinic
入组人数
30
试验地点
1
主要终点
Change in desmoid tumor symptom severity following ablation

研究概览

简要总结

This study will evaluate patient-reported outcomes before and after percutaneous ablation of desmoid tumors. Adult participants undergoing ablation for desmoid tumor will complete surveys pre and post procedure to assess symptom burden, impact on daily life, early post-procedural pain and recovery, concomitant treatments, and radiological response following ablation.

研究设计

研究类型
Observational
观察模型
Cohort
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
否

入选标准

  • •Adult patients undergoing ablation for desmoid tumor.

排除标准

  • •Declines to participate in research.

研究组 & 干预措施

Desmoid Tumor Ablation Cohort

Adult participants undergoing percutaneous ablation for desmoid tumor who complete patient-reported outcome surveys before and after treatment.

干预措施: Desmoid tumor ablation (Procedure)

结局指标

主要结局

Change in desmoid tumor symptom severity following ablation

时间窗: Baseline; 7 days; 1, 3, 6, 12, and 24 months post-ablation

Desmoid tumor symptom severity following ablation will be measured using the GODDESS© Desmoid Tumor Symptom Scale, a disease-specific patient-reported outcome measure assessing desmoid tumor-related symptoms. Scores will be calculated according to the validated GODDESS© scoring algorithm. Higher scores indicate greater symptom burden.

Change in desmoid tumor impact following ablation

时间窗: Baseline; 7 days; 1, 3, 6, 12, and 24 months post-ablation

Desmoid tumor impact following ablation will be measured using the GODDESS© Desmoid Impact Scale, a disease-specific patient-reported outcome measure assessing desmoid tumor-related symptoms on patients' daily lives and functioning. Scores will be calculated according to the validated GODDESS© scoring algorithm. Higher scores are expected to indicate greater disease-related impact.

Change in post-procedural pain score

时间窗: Baseline; 7 days; 1 month and 3 months post-ablation

The pain score is calculated from a 2 question self-report survey asking recipients to rate pain on a scale of 1-10. Higher scores indicate worse pain.

次要结局

  • Radiological response following ablation(Through 24 months post-ablation)

研究者

发起方
Mayo Clinic
申办方类型
Other
责任方
Principal Investigator
主要研究者

Rebecca Hibbert

Principal Investigator

Mayo Clinic

研究点 (1)

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