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Different Surgical Modalities for Thigh Lipodystrophy Including Liposuction,Thigh Lift and Liposuction Assisted Thigh Lift

Surgical Management of Thigh Lipodystrophy

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03283475
Acronym
thigh lift
Enrollment
90
Registered
2017-09-14
Start date
2017-05-14
Completion date
2019-04-01
Last updated
2017-09-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Thigh Lipodystrophy

Brief summary

The sample will be divided into two groups:- - Control group which will include 60 adult individuals between 18 and 35 years old who have BMI between 19 and 25, not complaining of any thigh contour deformities or skin redundancy with no history of body weight fluctuations. This group will be divided into two subgroups, 30 males and 30 females. The following measurements will be recorded :- Weight, height, thigh length, hip circumference, maximum buttocks circumference, upper thigh, middle thigh and lower thigh circumferences. \- Patient group which will include 40 patients suffering from thigh lipodystrophy and contour deformities who will undergo surgical intervention after their assessment. After assessment, one of the following techniques will be selected:- * Liposuction only. * thigh lift. * Liposuction assisted thigh lift.

Detailed description

Preoperative assessment:- Patients will be assessed regarding skin redundancy, history of weight loss and site of lipodystrophy whether deformity is proximal, distal or diffuse. The same measurements mentioned above will be recorded for the patient group before surgery. Preoperative photographs in anteroposterior, lateral and oblique positions will be taken. Informed consent will be signed by the patient before surgery illustrating possible risks and complications of the surgery. Postoperative assessment:- The outcomes will be evaluated 3 months after surgery regarding patient satisfaction and achievement of symmetry. Early complications will be assessed within one week after surgery including hematoma, seroma, surgical site infection and wound dehiscence. Late complications will be assessed at 3 months follow up including asymmetry, conspicuous scar and lymphedema. Postoperative measurements and photographs will be recorded and compared with preoperative ones.

Interventions

PROCEDUREthigh lift

liposuction-assisted medial avulsion thighplasty enables technically refined contouring of the thigh and the possible preservation of the local microvasculature, which results in reduced complication rates

Sponsors

Assiut University
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

The sample will be divided into two groups:- - Control group which will include 60 adult individuals between 18 and 35 years old who have BMI between 19 and 25, not complaining of any thigh contour deformities or skin redundancy with no history of body weight fluctuations. This group will be divided into two subgroups, 30 males and 30 females. The following measurements will be recorded :- Weight, height, thigh length, hip circumference, maximum buttocks circumference, upper thigh, middle thigh and lower thigh circumferences. \- Patient group which will include 40 patients suffering from thigh lipodystrophy and contour deformities who will undergo surgical intervention after their assessment. After assessment, one of the following techniques will be selected:- * Liposuction only. * thigh lift. * Liposuction assisted thigh lift.

Eligibility

Sex/Gender
ALL
Age
18 Years to 50 Years
Healthy volunteers
Yes

Inclusion criteria

1. Individuals between18 and 35 years for control group and more than 18 years for patient group . 2. Patients with BMI between 19 and 25 for control group and less than 35 for patient group.

Exclusion criteria

1. Individuals less than 18 years. 2. Patients undergoing bariatric surgery within a period of less than one year. 3. Patients with BMI more than 35. 4. Patients with systemic illness as cancer or mental disorders & hepatic patients (generally debilitating diseases) or any contraindication for anesthesia.

Design outcomes

Primary

MeasureTime frameDescription
regarding patient satisfaction and achievement of symmetry.3 monthsquestionnaire will be performed for the patient group to estimate degree of patient satisfaction with assessment of postoperative symmetry

Secondary

MeasureTime frameDescription
complication rates of different surgical techniques1 week and 3 monthsEarly complications will be assessed within one week after surgery including hematoma, seroma, surgical site infection and wound dehiscence. Late complications will be assessed at 3 months follow up including asymmetry, conspicuous scar and lymphedema.

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026