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临床试验/NCT06269055
NCT06269055已完成不适用

Long-term Result of DTPA Chelation for Gadolinium Deposition Disease

Stanford University1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2024年12月2日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
30
试验地点
1
主要终点
Rating of Gadolinium Deposition Disease Symptoms at start of GDD and currently

研究概览

简要总结

This study is aimed at describing the degree of benefit, if any, and the adverse effects, if any, from receiving 5 or more treatment sessions of Gadolinium Deposition Disease using two-day chelation treatment with the chelating agents Calcium Diethylenetriamine pentaacetate (Ca-DTPA) and Zinc Diethylenetriamine pentaacetate (Zn-DTPA).

详细描述

Potential participants will be invited to contact Dr. Koran by email to receive a telephone screening Informed Consent. Those who provide informed consent will have their questions about the study answered and their interest and eligibility assessed via telephone interview. Those who wish to participate will be sent an Informed Consent for study participation. Those who return the consent will be sent four study questionnaires for completion and return. The returned forms will be reviewed by Dr. Koran or his co-investigator, and a follow-up phone call will be offered via Secure Stanford email. The phone call will involve answering any new questions the participant has, and clarifying the participant's responses to the data collection forms if clarification is needed. Participants who wish to receive a summary of the study's results once it is completed and accepted for publication, will be emailed a summary via Secure Stanford email.

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Retrospective

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

  • •Age 18 or older,
  • •Diagnosis of Gadolinium Deposition Disease (GDD) established by treating MD according to current criteria and confirmed by investigator review of screening questionnaire (dx criteria: presence of at least 3 of 8 symptoms-cognitive disturbance, extremity pain, arthralgia, chest wall pain, skin pain, headache, skin induration, and skin hyperpigmentation; and, had an unprovoked 24-hour Gd urine excretion level exceeding the laboratory norm at least 28 days after the symptom-inducing MRI;
  • •has had five or more 2-day chelation treatments with Ca-DTPA/Zn-DTPA;
  • •will be at least 2 weeks post the last chelation treatment at the time of completing the patient data-gathering questionnaires.
  • •no more than 2 years have elapsed since the last DTPA chelation.

排除标准

  • •1. Not fluent in written and spoken English;
  • •having impaired hearing that significantly decreases the person's ability to communicate via telephone;
  • •Unable to provide informed consent;
  • •Participating or having participated in protocols involving a pharmacological treatment of GDD other than DTPA chelation. Note: brief pre- or post-DTPA chelation to prevent GDD symptom flare is not an exclusion criterion.

结局指标

主要结局

Rating of Gadolinium Deposition Disease Symptoms at start of GDD and currently

时间窗: Two or more weeks after the last of 5 of more DTPA chelation treatments

Patient-completed data regarding symptoms experienced and their intensity when they began and currently, rated from 0 (none) to 5 (very severe). Outcome measure will be change in each symptom's intensity.

次要结局

  • PROMIS Item Bank v2.0 - Cognitive Function- Short Form 8a(Past 7 days)
  • Sheehan Disability Scale(Past week)

研究者

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

Lorrin M Koran, MD

Professor of Psychiatry and Behavioral Sciences

Stanford University

研究点 (1)

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