Lipedema

15

Review clinical trials related to Lipedema. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Efficacy of Complex Decongestive Therapy, Exercise and Diet in Women With Lipedema

The purpose of this study is to compare the effectiveness of standard physical therapy methods (Complex Decongestive Therapy, Pneumatic Compression, and Exercise) combined with two different nutritional approaches (personalized anti-inflammatory diet vs. standard healthy nutrition education) in women diagnosed with lower extremity lipedema.

Participants needed: 75
Trial details
Age: 18-65Biological sex: FemaleType: InterventionalSponsor: Balikesir UniversityUpdated: Jun 25, 2026Locations: 1
Eligibility criteria

Female, aged 18 to 65 years. [+3]

Presence of active malignancy. [+9]

Status: Not yet recruiting

Serum Maresin-1 Levels in Patients With Lipedema: A Cross-Sectional Study

Lipedema is a chronic and progressive adipose tissue disorder characterized by symmetrical fat accumulation, pain, tenderness, and easy bruising, predominantly affecting women. Increasing evidence suggests that chronic low-grade inflammation and impaired resolution of inflammation may contribute to its pathophysiology. Maresin-1 is a specialized pro-resolving lipid mediator with potent anti-inflammatory and tissue-protective properties; however, its role in lipedema remains largely unknown. This cross-sectional observational study aims to evaluate serum Maresin-1 levels in women with lipedema and to investigate their associations with pain severity, inflammatory markers, central sensitization, and quality of life. Serum Maresin-1 levels and clinical characteristics will be compared among women with lipedema, obese women without lipedema, and healthy controls to explore the potential value of Maresin-1 as a biomarker in lipedema.

Participants needed: 84
Trial details
Age: 18-65Biological sex: FemaleType: ObservationalSponsor: Kanuni Sultan Suleyman Training and Research HospitalUpdated: Jun 16, 2026
Eligibility criteria

Female participants aged 18 to 65 years. Women with a clinical diagnosis of lipe...

Active infection at the time of enrollment. History of autoimmune or chronic inf...

Status: Not yet recruiting

Assessment of Venous Insufficiency and Clinical Features in Lipedema

Lipedema is a chronic adipose tissue disorder characterized by disproportionate fat accumulation, pain, tenderness, edema, and functional impairment. Venous symptoms such as heaviness, swelling, and discomfort are frequently reported in individuals with lipedema; however, the relationship between venous Doppler ultrasonography findings and lipedema-related clinical manifestations remains insufficiently investigated. This cross-sectional controlled study aims to evaluate venous insufficiency parameters in patients with lipedema using Doppler ultrasonography and to examine their associations with pain severity, lower extremity function, disease severity, and quality of life.

Participants needed: 82
Trial details
Age: 18-65Biological sex: FemaleType: ObservationalSponsor: Sultan Abdulhamid Han Training and Research Hospital, Istanbul, TurkeyUpdated: May 22, 2026Locations: 1
Eligibility criteria

Female participants aged 18 years or older [+3]

History of lower extremity venous surgery or sclerotherapy [+8]

Status: Not yet recruiting

The Effect of Lipedema on Knee Osteoarthritis

This study will be one of the few to examine the effect of lipedema on knee osteoarthritis in a comparative manner with a control group within the same osteoarthritis context. Although the relationship between obesity and osteoarthritis has been extensively studied in the literature, the effect of specific adipose tissue pathologies, such as lipedema, on osteoarthritis has not been sufficiently investigated. This study aims to demonstrate the independent effect of lipedema on osteoarthritis, evaluate clinical and ultrasonographic parameters together, and contribute to early diagnosis and targeted rehabilitation strategies.

Participants needed: 76
Trial details
Age: 30-65Biological sex: FemaleType: ObservationalSponsor: Izmir Democracy UniversityUpdated: May 8, 2026Locations: 1Duration: 1 Day
Eligibility criteria

Women aged 30-65 [+6]

Inflammatory arthritis [+10]

Status: Recruiting

Multimodal Ultrasound for Differentiating Lymphedema and Lipedema

The aim of this observational study is to evaluate the diagnostic value of multimodal ultrasonography in differentiating between lymphedema and lipedema. Differentiating these two chronic conditions based solely on clinical examination can be challenging due to overlapping symptoms. This study will utilize various non-invasive ultrasound techniques-including B-mode ultrasound, strain elastography, power Doppler, and quantitative ImageJ analysis-to compare tissue characteristics among patients with lymphedema, patients with lipedema, and healthy controls. The goal is to identify reliable, non-invasive imaging biomarkers that can facilitate early and accurate diagnosis, thereby optimizing patient management.

Participants needed: 75
Trial details
Age: 18-75Biological sex: FemaleType: ObservationalSponsor: Kayseri City HospitalUpdated: Mar 24, 2026Locations: 1
Eligibility criteria

Not listed

Status: Recruiting

The Impact of Metabolic Status on Pain and Central Sensitization in Women With Lipedema: A Cross-Sectional Observational Study

The aim of this study is to evaluate the effect of metabolic markers (HOMA-IR, triglyceride/HDL ratio, HbA1c, waist and hip circumference measurements, BMI, etc.) on pain and central sensitization in patients diagnosed with lipedema. The primary objective is to investigate the association between metabolic markers and central sensitization. The secondary objective is to assess the relationship between metabolic markers and pain intensity, pain phenotype, and functional status.

Participants needed: 59
Trial details
Age: 18+Biological sex: FemaleType: ObservationalSponsor: Marmara UniversityUpdated: Mar 12, 2026Locations: 1
Eligibility criteria

Being female and aged 18 years or older [+3]

Presence of a history of malignancy, active infection, inflammatory rheumatic di... [+12]

Status: Available

Effect of Ultrasound Cavitation Versus Pneumatic Compression on Adipose Tissue Thickness on Lipedema Patients

PURPOSE: This study will be conducted to investigate any significant effect of ultrasound fat cavitation or pneumatic compression on adipose tissue thickness in patients with lipedema. BACKGROUND: Lipedema is a connective tissue disorder that cause physical discomfort and psychological stress. A literature review published in 2020 estimated that 10-11% of women or approximately 400 million women across the globe have lipedema. Lipedema fat is dangerous when it progress onto abdomen and trunk resulting in a risk of developing high blood pressure, high cholesterol and diabetes. Ultrasound cavitation is a safe cosmetic procedure has almost no adverse reactions used to break down fat cells under the skin which improves the body shape and reduce circumference which make it a promising non invasive tool alternative to surgical liposuction. Pneumatic compression is bl=elieved to reduce the limb circumference and volume which make it a good treatment option for lipedema. HYPOTHESES: Null Hypothesis:there will be no significant effect of fat cavitation or pneumatic compression on the adipose tissue thickness in patients with lipedema. RESEARCH QUESTION:Will be any significant effect of fat cavitation or pneumatic compression on the adipose tissue thickness in patients with lipedema

Trial details
Age: 30-45Biological sex: FemaleType: Expanded AccessSponsor: Cairo UniversityUpdated: Feb 11, 2026Locations: 1
Eligibility criteria

Ninety females patients their age from 30 to 45 years [+2]

Patents with severe lipedema [+6]

Status: Recruiting

Investigation of Medial Longitudinal Arch and Foot Function in Patients With Lipedema

Lipedema is a chronic adipose tissue disorder that commonly leads to joint laxity, hypermobility, and functional limitations, yet its impact on foot morphology has not been systematically examined. This case-control study aims to investigate whether patients with lipedema exhibit a higher prevalence of generalized joint hypermobility and foot structural abnormalities-specifically pes planus-compared with age- and BMI-matched controls. Using radiographic measurements (Meary angle and calcaneal inclination angle), clinical hypermobility assessment, and validated functional scales, the study seeks to determine the relationship between lipedema, hypermobility, and foot function.

Participants needed: 32
Trial details
Age: 18-65Biological sex: FemaleType: ObservationalSponsor: Marmara UniversityUpdated: Jan 2, 2026Locations: 1
Eligibility criteria

Female participants [+7]

Pregnancy [+6]

Status: Not yet recruiting

Investigation of the Effects of High-Intensity Interval Exercise and Moderate-Intensity Continuous Exercise on Limb Volume, Functional Capacity, and Quality of Life in Patients With Lipedema

This randomized controlled clinical study aims to investigate and compare the effects of high-intensity interval training (HIIT) and moderate-intensity continuous training (MICT), when combined with intermittent pneumatic compression (IPC) therapy, on limb volume, functional capacity, pain, fatigue, anxiety, depression, sleep quality, and quality of life in women with lipedema. Lipedema is a chronic, progressive adipose tissue disorder primarily affecting women, characterized by abnormal and symmetrical fat accumulation in the lower extremities that does not improve with weight loss or limb elevation. It is often misdiagnosed as obesity or lymphedema, leading to delayed treatment. Lipedema causes pain, swelling, bruising, mobility limitation, and reduced quality of life. Conservative treatment options include compression therapy, manual lymphatic drainage, and exercise. IPC is a non-invasive treatment used to reduce limb volume and pain while improving function and quality of life. Exercise is also a cornerstone of conservative management, but the optimal exercise intensity for lipedema remains unclear. In this study, 69 female patients aged 18-65 years diagnosed with lipedema according to Halk and Damstra criteria will be randomly assigned into three groups: IPC + Home-based walking program IPC + High-Intensity Interval Training (HIIT) IPC + Moderate-Intensity Continuous Training (MICT) All participants will receive 15 IPC sessions (3 times per week for 5 weeks). The exercise programs (HIIT or MICT) will continue for 10 weeks, supervised by a physiotherapist. The home-based group will be encouraged to walk ≥10,000 steps daily using a pedometer application. Primary outcome: Change in limb volume measured by circumferential measurements and the truncated cone formula. Secondary outcomes: Pain (VAS), functional capacity (6-Minute Walk Test), muscle strength (dynamometry), pressure pain threshold (algometry), physical activity (IPAQ-SF), lower extremity function (LEFS), quality of life (SF-12), sleep quality (PSQI), fatigue (FSS), and anxiety/depression (HADS). Measurements will be taken at baseline (T0), after 15 IPC sessions (T1), and after 30 total sessions or 10 weeks (T2). The investigators hypothesize that both HIIT and MICT combined with IPC will provide superior improvements in physical and psychological outcomes compared to IPC with a home-based walking program alone.

Participants needed: 69
Trial details
Age: 18-65Biological sex: FemaleType: InterventionalSponsor: Marmara UniversityUpdated: Jan 6, 2026Locations: 1
Eligibility criteria

Female participants aged 18-65 years [+2]

Pregnancy or breastfeeding [+5]

Status: Recruiting

Vascular Lab Resource (VLR) Biorepository

This is a study of biomarkers obtained from prospectively collected subject samples and their correlation with cardiovascular and metabolic diseases. The purpose of this initiative is to develop an enduring tool to allow for collaborative research between clinicians at Cleveland Clinic Main Campus and basic scientists at the Lerner Research Institute. This collaboration will allow resources to be available to clinical and basic researchers alike. This tool will enable research of vascular disease in the Vascular Lab and will leverage this valuable asset to the fullest extent to allow for interdepartmental collaboration.

Participants needed: 500
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: The Cleveland ClinicUpdated: Dec 19, 2025Locations: 1
Eligibility criteria

18 years or older [+2]

Known life expectancy of ≤ 6 months at the time of enrollment [+2]

Status: Not yet recruiting

ESWT for Primary Lipedema

This randomized controlled clinical trial aims to evaluate the effectiveness of extracorporeal shockwave therapy (ESWT) when added to standard conservative treatment in women with primary lipedema. Participants will be randomly assigned to receive either standard conservative therapy alone or standard therapy combined with radial ESWT. The study will assess changes in pain intensity (VAS), limb circumference measurements, quality of life (SF-36), and patient satisfaction over an 8-week period. Evaluations will be performed at baseline, at the end of the 4-week treatment phase, and at 4-week follow-up. This trial seeks to provide evidence on whether ESWT offers additional clinical benefit in the management of primary lipedema.

Participants needed: 50
Trial details
Age: 18-65Biological sex: FemaleType: InterventionalSponsor: Fatih BagcierUpdated: Nov 20, 2025
Eligibility criteria

Not listed

Status: Recruiting

Investigation of Central Sensitization and Associated Factors in Patients With Lipedema

This study aims to investigate the presence of central sensitization and its associated parameters in patients with lipedema. Lipedema is a chronic and hereditary condition that primarily affects the lower extremities in women and is often associated with hormonal changes. Symptoms such as pain, swelling, and tenderness are common in lipedema, and these symptoms may be related to central sensitization. Additionally, the ultrasonographic findings and pain sensitivity in lipedema will be compared with those of healthy individuals. This study seeks to contribute to the diagnosis and treatment process of lipedema.

Participants needed: 50
Trial details
Age: 18-65Biological sex: AllType: ObservationalSponsor: Sultan Abdulhamid Han Training and Research Hospital, Istanbul, TurkeyUpdated: Sep 8, 2025Locations: 1
Eligibility criteria

Lipedema; Diagnosis of lipedema Aged between 18 and 65 years Literate Willing to... [+1]

Lipedema group; Under 18 or over 65 years of age Presence of concurrent lymphede... [+1]

Status: Recruiting

Proof of Concept, Randomized, and Crossover Study, to Assess the Effectiveness of Two Types of Compression Garments in Lipedema

The goal of this prospective randomized crossover experimental study is to assess the effectiveness and tolerance of circular and flat fabric garments in stabilizing lower-limb volume in lipedema. It will assess the effectiveness of the garments and determine any differences between both types of hosiery currently used in routine clinical practice. Participants will be prescribed either circular or flat-knitted pantyhose and wear them daily for 6 months. After 6 months, they will change the type of garment.

Participants needed: 34
Trial details
Age: 18-70Biological sex: FemaleType: InterventionalSponsor: Isabel Forner-Cordero, MD, PhDUpdated: May 14, 2025Locations: 1
Eligibility criteria

Clinical diagnosis of lipedema: increased lowe-limb volume, disproportion betwee... [+5]

Lipedema with fatty lobulations. [+9]

Status: Recruiting

Sarcopenia and Related Factors in Lipedema

Lipedema is a common disease of subcutaneous adipose tissue. The most common complaint of patients with swelling in the affected extremity is pain. In addition, patients with lipedema may experience conditions that can greatly affect the health and quality of life of the individual, such as loss of muscle strength and exercise capacity, and deterioration in activity levels of daily living. It is still unknown whether the decrease in muscle strength in patients with lipedema is part of this condition or whether decreased activity levels lead to decreased muscle strength. Sarcopenia is an important health problem characterized by age-related loss of muscle mass and muscle function. The relationship between muscle weakness and sarcopenia in patients with lipedema has not been investigated before. Early recognition of possible sarcopenia and functional limitations in these patients may be important to increase the ability of patients to participate in physical activity as part of their conservative management. There is no study in the literature investigating sarcopenia in patients with a diagnosis of lipedema. The aim of this study is to evaluate patients with a diagnosis of lipedema in terms of sarcopenia. In addition, the relationship between sarcopenia and age, body mass index, exercise frequency, lipedema type, and stage will be investigated in patients diagnosed with lipedema.

Participants needed: 102
Trial details
Age: 18-85Biological sex: FemaleType: ObservationalSponsor: Dokuz Eylul UniversityUpdated: Mar 12, 2025Locations: 1
Eligibility criteria

between the ages of 18-85 [+4]

with chronic venous insufficiency and/or lymphedema [+2]

Status: Recruiting

Effects of Exercise in Patients with Lipedema

Lipedema is a chronic progressive disease characterized by symmetrical, disproportionate swelling of subcutaneous adipose tissue, which is common in women and mostly seen in the lower extremities and to a lesser extent in the upper extremities. Healthy lifestyle approaches including exercise treatments are very important for lipedema patients in order to prevent disease progression. The aim of this study is to investigate the effects of exercise on edema, pain, exercise capacity, lower extremity muscle strength and function in lipedema patients. Sociodemographic information of the patients, body composition with Tanita InnerScan BC-601-CG device, clinical information regarding lipedema, type and stage of lipedema, inspection, palpation findings will be recorded. Local tissue water percentage will be assessed using Moisturemeter-d compact (MMDc, Delfin Technologies, Kuopio, Finland) device, circumference measurement using tape, pain intensity with Visual Analog Scale, pain threshold with Baseline brand digital algometer device. Muscle strength will be assessed using K-Force hand dynamometer. Functional exercise capacity will be assessed with the 6-minute walk test (6MWT), and lower extremity dysfunction with the lower extremity functional scale. After the assessments are made, the patients will be randomly divided into 2 groups. The patients in the study group will perform group exercises consisting of warm-up, loading and cool-down periods of 40-50 minutes, 2 days a week for 6 weeks, and strengthening exercises applied to the hip muscles and knee extensors with elastic resistance bands, which are decided according to the level of effort perceived by the patient, 3 sets of 10 repetitions, 2 days a week for 6 weeks. The same assessments will be applied to the patients again at the end of the exercise program. The control group will be re-evaluated after 6 weeks with suggestions regarding lipedema and physical activity level, and the obtained data will be compared.

Participants needed: 20
Trial details
Age: 18+Biological sex: FemaleType: InterventionalSponsor: Ilke KeserUpdated: Feb 6, 2025Locations: 1
Eligibility criteria

Having a diagnosis of Lipedema, [+1]

Individuals with cardiopulmonary, rheumatic or neurological diagnoses that have... [+3]