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EFFECTIVENESS OF ULTRASOUND FOR LOCAL FAT TREATMENT (n)

S

São Paulo State University

Status

Unknown

Conditions

Fat Burn

Treatments

Procedure: ultrassound

Study type

Interventional

Funder types

Other

Identifiers

NCT04043182
SaoPSU_univar

Details and patient eligibility

About

It's evident that the literature shows good results on the use of aesthetic ultrasound in the treatment of localized fat, however, little has been explored so far, about possible psychological influences of this method and therefore, it is believed that it is pertinent to elaborate studies that include a placebo group, in order to measure the real effects from the exclusive application of ultrasound. Therefore, the objective of this study will be to verify the influence of the application of aesthetic ultrasound in the treatment of localized fat, using for both clinical, biochemical and functional parameters.

Full description

There will be included 30 participants, female gender, communities between 18 and 30 years, apparently Saudi, local abdominal fat, located in three groups: control (n = 10), experimental (n = 10) and placebo (n = 10) . Or group control não recebeu nenhum type of intervention. No experimental group, 10 sessões de ultrassom (Skinner brand, São Paulo) will be carried out in the previous region for 20 minutes. No placebo group will be applied ultrassom (Skinner brand, São Paulo), pormem com zerada intensities. Anthropometric avaliação e of dobras cutâneas will be carried out at this time before applying the treatment protocol. As skin folds will be measured by means of adipometers.

Enrollment

30 estimated patients

Sex

Female

Ages

18 to 30 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Additional inclusion criteria included body mass index (BMI) equal to or less than 25.0 kg / m2
  • Adipose tissue thickness 2.6 cm or more in the treatment region;
  • Preserved elasticity and local tissue integrity;
  • In addition, participants had to agree not to change their daily routines during the study.

Exclusion criteria

  • Pregnancy.
  • Breastfeeding;
  • History of liposuction;
  • Lipolysis by injection therapy;
  • Abdominoplasty or surgery in the treatment region;
  • Weight reduction medication;
  • Recent surgery in the last 12 months;
  • Implantable electrical device;
  • Neurosurgical deviation;
  • Hernia;
  • Sensory loss or dysesthesia in the treatment region;
  • Cancer;
  • Circulation problems;
  • Or chronic systemic disease such as diabetes or metabolic syndrome.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

30 participants in 3 patient groups, including a placebo group

group control
No Intervention group
Description:
You will not receive any type of intervention
treatment group (ultrasound)
Experimental group
Description:
Will perform protocols of 10 sessions of ultrasound in the region of abdomen
Treatment:
Procedure: ultrassound
placebo group
Placebo Comparator group
Description:
It will perform protocols of 10 sessions of ultrasound in the region of abdomen, but the apparatus will be with zero intensities
Treatment:
Procedure: ultrassound

Trial contacts and locations

1

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Central trial contact

Jaqueline Lopes, master; Aryane Machado, PHD

Data sourced from clinicaltrials.gov

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