Cellulitis Clinical Trial
Official title:
Effect of Vibro-oscillatory Therapy for Improvement of Body Contour and Appearance of Cellulite.
OBJECTIVE: To evaluate the efficacy of vibro-oscillatory therapy through an electromedical
equipment in improving body contour and appearance of cellulite.
SUBJECTS AND METHODS: A prospective and comparative longitudinal clinical study will be
performed in 30 women with cellulitis. Patients will be submitted to data collection and
evaluation and before and after vibration-oscillatory therapy.
HYPOTHESES: Patients are expected to show improvement in body contour and cellulite after
vibration-oscillatory therapy.
STATISTICAL ANALYSIS: A descriptive analysis will be done before and after
vibration-oscillatory therapy, with frequency tables for categorical and descriptive
variables (mean, standard deviation, median, minimum and maximum values) for continuous or
numerical variables. In order to compare the main variables between the groups and the
collection times, the analysis of variance (ANOVA) for repeated measures will be used.
Tukey's test will be used to compare the groups. The significance level adopted for the
statistical tests will be 5% or p <0.05.
After approval by the institutional committee of Research Ethics, the subjects will be
approached by the researcher responsible on the day of their evaluation, where they completed
the registration form, after a brief analysis of the inclusion and exclusion criteria of the
present study, the individuals included in the study will be collection of anthropometric
data: weight, height, BMI, perimeter of the treated region, assessment of the degree of
gynoid lipodystrophy, clinical inspection and photographic study of the treated area,
ultrasound examination to assess the thickness of the dermis and hypodermis and the
examination with Cutometer ® to assess the viscoelasticity of the skin.
Patients will be divided according to the degree of cellulite they present and will be
treated with vibration therapy, such as the Modellata® electromedical equipment (Ibramed-
Brazilian Industry of Electronic Equipment), being performed three times a week for two
months totaling 16 sessions by a dermato-functional physiotherapist.
Data collection and evaluation will be performed before and after treatment.
;
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT02864420 -
Hospitalization at Home: The Acute Care Home Hospital Program for Adults
|
N/A | |
Completed |
NCT00746109 -
Study of Wound Packing After Superficial Skin Abscess Drainage
|
Phase 4 | |
Completed |
NCT03296280 -
Evaluation of Implementation of a National Point-of-Care Ultrasound Training Program
|
||
Not yet recruiting |
NCT01947660 -
Continuous Regional Anesthesia for Septic Limb Orthopedic Surgery
|
N/A | |
Completed |
NCT01876628 -
Adjunctive Clindamycin for Cellulitis: C4C Trial.
|
Phase 4 | |
Active, not recruiting |
NCT01706913 -
Study Assessing Impact of Dermatology Consultation for Patients Admitted With Cellulitis
|
N/A | |
Completed |
NCT03474523 -
Effectiveness of Diathermy-Radiofrecuency Compared With Cavitation in Cellulitis Treatment
|
N/A | |
Active, not recruiting |
NCT05226260 -
Decreasing Antibiotic Duration for Skin and Soft Tissue Infection Using Behavioral Economics in Primary Care
|
N/A | |
Active, not recruiting |
NCT03785834 -
The Effect of Histopathologic Analysis and Tissue Cultures on Inpatient Management of Cellulitis and Pseudocellulitis
|
||
Completed |
NCT01549613 -
Evaluation of Daptomycin for the Emergency Department Treatment of Complicated Skin and Skin Structure Infections
|
Phase 4 | |
Completed |
NCT01029782 -
Comparison of Intravenous Cefazolin Plus Oral Probenecid With Oral Cephalexin for the Treatment of Cellulitis
|
Phase 2 | |
Completed |
NCT00676130 -
Study of New Antibiotic Regimen for the Treatment of Uncomplicated Cellulitis in Emergency Department Patients
|
N/A | |
Not yet recruiting |
NCT03917134 -
Prevention of Vaginal Cellulitis or Vaginal Cuff Abscess After Laparoscopic Hysterectomy
|
N/A | |
Completed |
NCT02230813 -
Predictors of Oral Antibiotic Treatment Failure in Emergency Department Patients With Cellulitis
|
N/A | |
Completed |
NCT01557426 -
Soft Tissue Ultrasound of Infections
|
Phase 1 | |
Completed |
NCT01339091 -
Efficacy and Safety of Dalbavancin for the Treatment of Acute Bacterial Skin and Skin Structure Infections
|
Phase 3 | |
Completed |
NCT00984022 -
Aquacel Versus Iodoform Gauze for Filling Abscess Cavity Following Incision and Drainage
|
Phase 2 | |
Completed |
NCT04091672 -
RECELL® System Combined With Meshed Autograft for Reduction of Donor Skin Harvesting in Soft Tissue Reconstruction
|
N/A | |
Completed |
NCT05023200 -
The Personalised Antibiotic Duration for Cellulitis (PAD-C) Study
|
||
Terminated |
NCT02087527 -
Use of Corticosteroids in Children With Cellulitis
|
N/A |