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Clinical Trials/DRKS00031411
DRKS00031411
Recruiting
Not Applicable

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

niversität zu Köln0 sites150 target enrollmentMarch 6, 2023

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
ipohyperplasia dolorosa, Lipedema
Sponsor
niversität zu Köln
Enrollment
150
Status
Recruiting
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
March 6, 2023
End Date
TBD
Last Updated
last year
Study Type
Observational
Sex
Female

Investigators

Sponsor
niversität zu Köln

Eligibility Criteria

Inclusion Criteria

  • 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\.

Exclusion Criteria

  • 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

Outcomes

Primary Outcomes

Not specified

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