跳至主要内容
临床试验/DRKS00031411
DRKS00031411招募中不适用

ongitudinal characterization of the sensory phenotype of lipohyperplasia dolorosa (LiDo) patients during weight loss and subsequent liposuction.

niversität zu Köln0 个研究点目标入组 150 人开始时间: 2023年3月6日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
150

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18 Years 至 40 Years(—)
性别
Female

入选标准

  • Generally: female, age between 18-40 years, present signed and irrevoked informed consent.
  • For LiDo patients for weight reduction: medical diagnosis Lipohyperplasia dolorosa (LiDo), coincident obesity BMI > 40,
  • For the weight loss group: study-independent planned weight loss to achieve BMI <40 required for lymphatic liposculpture.
  • For LiDo patients for lymphologic liposculpture: physician diagnosis of lipohyperplasia dolorosa (LiDo),
  • For the surgery group: lymphological liposculpture planned for study-independent reasons, no coincident obesity; BMI <40.
  • For obese patients: No medical diagnosis of lipohyperplasia dolorosa (LiDo), obesity BMI > 40.

排除标准

  • Limitation of the ability to communicate (language barrier, cognitive barriers, ...).
  • Diseases affecting the sensory nervous system (e.g. Parkinson's disease, multiple sclerosis, radiculopathy, injuries of nerves innervating the sensory area of different genesis, diabetic polyneuropathy, peripheral polyneuropathies of different genesis, etc.).
  • skin stresses on the areas of measurement
  • topical application of analgesics to the areas of measurement (e.g. plasters, creams, ...)
  • diagnosed coagulation or wound healing disorder
  • other known alteration in pain perception or another diagnosed pain disorder
  • Liposuction already performed prior to study inclusion

研究者

发起方
niversität zu Köln

相似试验