Obesity, Morbid Clinical Trial
— LIPODIETOfficial title:
Effect of an Low Carbon High Fat Diet on Pain- and Quality of Life in Patients With Lipedema
Verified date | February 2019 |
Source | Central Norway Regional Health Authority |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Lipedema is a chronic disease with unproportional, symmetrical fat accumulation in the lower extremities. Patients experience pain in affected areas, and reduced quality of life. Today's treatment is physiotherapy and surgery (liposuction). Recent research shows that ketogenic-diet with low carbohydrate, high fat (LCHF) conant can lead to reduced pain, increased quality of life and change in body composition. Goals: Investigate the effect of LCHF diet on pain, quality of life and body composition.
Status | Completed |
Enrollment | 10 |
Est. completion date | January 10, 2019 |
Est. primary completion date | January 10, 2019 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 18 Years to 75 Years |
Eligibility |
Inclusion Criteria: - weight stable over the last three months (+ 2-3 kg) - not currently dieting to loose weight. - willing to meet for weekly follow-ups during the intervention and the reintroduction of a regular diet. - sign an informed consent before entering the study. Exclusion Criteria: - pregnant or breast feeding - history of infectious diseases - medication known to affect obesity - enrolment in any other obesity treatment - have had a bariatric surgery - history of psychological disorders - mentally disabled - not mastering a Scandinavian language - having a malign disease or any disease that leads to dietary advice that is not consistent with intervention advices in the study |
Country | Name | City | State |
---|---|---|---|
Norway | Obesity Clinic, St Olavs Hospital | Trondheim |
Lead Sponsor | Collaborator |
---|---|
Central Norway Regional Health Authority | St. Olavs Hospital, University of Oslo |
Norway,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Lymphedema Quality of Life questionnaire | 6 weeks | ||
Primary | Pain indicated on a visual analog scale | 6 weeks |
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