跳至主要内容
临床试验/CTIS2024-513529-21-00
CTIS2024-513529-21-00进行中(未招募)1 期

Basic Toolbox for Lipedema Syndrome Assessment (BATOLISA)

niversite Libre de Bruxelles0 个研究点目标入组 60 人开始时间: 2024年5月9日最近更新:
适应症

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
60

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

年龄范围
18 至 64(—)

入选标准

  • Inclusion criteria for LIPEDEMA PATIENTS: 1. Women, Age: 18-50 y.o. (non-menopausal), Signed informed consent form, BMI: 18-30, Waist to hip ration /=4, Lipedema syndrome diagnosed by a health professional, Inclusion criteria HEALTHY SUBJECTS - 1-4 AS ABOVE (1. women; 2. age: 18-50 (non menopausal); 3. BMI: 18-300; 4. Signed informed consent form

排除标准

  • Allergy to iodine or shellfish, Oncologic history, Hyperthyroïdisme, Autonomus thyroid adenoma, Hypersensitivity to Indocyanine green, Skin lesions, Male subjects, Menopause or perimenopause period, Pregnancy, Breastfeeding, Refusal and/or incapacity to give informed consent form, Advanced renal impairment, Known coagulation disorders, Use of anticoagulants

研究者

发起方
niversite Libre de Bruxelles

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