跳至主要内容
临床试验/NCT01438047
NCT01438047撤回不适用

OFDI in Dermatology

Massachusetts General Hospital1 个研究点 分布在 1 个国家开始时间: 2010年9月最近更新:
适应症

试验速览

阶段
不适用
状态
撤回
试验地点
1
主要终点
OFDI in Dermatology - Change from baseline in vascular density

研究概览

简要总结

This is a pilot exploratory study. The goal of this study is to evaluate a new imaging tool, optical frequency domain imaging (OFDI), to reveal the microvascular morphology of capillary malformations.

详细描述

The subject population will be composed of 8 subjects meeting the inclusion and exclusion criteria. Up to 8 subjects may be enrolled for the study after obtaining written, informed consent prior to participation in the study. Recruitment will be performed by direct advertisement to subjects inside and outside Brigham and Women's Hospital (BWH), including the BWH dermatology clinic. The study patients will be managed using standard of care in practice at the BWH dermatology clinic. The study will be conducted at Brigham and Women's Hospital Dermatology Clinic where the pulsed dye laser is housed.

Patients referred to the BWH dermatology clinic will be eligible for recruitment. The study nurse/staff involved in patient enrollment will be familiar with the care of this type of patients. The medical history of these patients will be examined to determine if the study eligibility requirements are met. If the patient is selected as a potential subject, a letter will be sent about 7 days prior to their scheduled exam to ask if they would care to participate. This time frame should allow time for the patient to consider study participation.

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 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Subjects: Fitzpatrick skin type I-VI, of either gender
  • Subjects must be between 18 and 80 years of age.
  • Subjects must have a not previously treated port wine stain of at least 1 cm2 on either a) trunk and extremities or b) face and neck.
  • Subjects are scheduled for PLD treatment of the port wine stain
  • Subjects must be willing and able to comply with all follow-up requirements.

排除标准

  • Subjects must not have active localized or systemic infections
  • Subjects must not be on aspirin.
  • Subjects must not be currently taking Accutane or be off Accutane for less than 6 months prior to initiation of the study.
  • Subjects must not be participating in potentially confounding research; e.g. a clinical study of any other unapproved investigational drug or device.
  • Subjects must not be pregnant or planning to become pregnant over the course of the study.

结局指标

主要结局

OFDI in Dermatology - Change from baseline in vascular density

时间窗: 4 weeks

There will be four times the patient is imaged using OFDI. Imaging is done to measure the vascular density within the specified area that is imaged. The first time imaging takes place is immediately prior to PDL treatment. The second in immediately following the treatment. The third and fourth imagings will be taken approximately four weeks after the initial visit. At this second visit the patient will have their second and final PDL treatment. An image will be take prior and following the PDL treatment.

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

Benjamin Vakoc

Assistant Professor

Massachusetts General Hospital

研究点 (1)

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