NCT02185950

Brief Summary

Burning produces changes in the biomechanical properties of the skin causing limitation of movement. The increase in skin suppleness is very important in the rehabilitation process, since its increase makes therapeutic interventions aimed at increasing the range of motion, thus improving functional pattern. Will be evaluated 60 volunteers of both sexes aged 20-80 years seen at the Burns Unit of the Clinical Hospital of the Faculty of Medicine of Ribeirão Preto. There will be a traditional physical therapy evaluation as well as evaluation of the specific characteristics of the burn and scar. The temperature of the region will be assessed by thermography, and biophysical parameters and biomechanical skin evaluated by Cutometer and their accessory probes (mexameter, reviscometer, sebometer) before, immediately after and 10, 20 and 30 minutes of application of therapeutic resources. Volunteers will undergo continuous application of ultrasound with 3 MHz and intensity of 1 W/cm2 in the region due to scar deep second degree burn or third degree, and the application time of 2 minutes for each effective radiation area of the head (ERA) in a predetermined region of 9X5 cm a total of 4 minutes of application, therapy paraffin 20 minutes and 4 minutes endermology negative pressure between 100 and 200mmHg, in a continuous mode with glass head (1.5cm in diameter .) Applications will be set by random draw (design crusader cross-over) with an interval of 7 days between applications (wash-out). The data will be submitted to analysis of normality by the Shapiro-Wilk test, and the behavior of the effect between groups and pre-and post-intervention will be evaluated by two-way ANOVA followed by post-hoc (Bonferroni) or Friedman, p \<0.05

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
60

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Jun 2012

Longer than P75 for not_applicable

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

June 1, 2012

Completed
1.2 years until next milestone

First Submitted

Initial submission to the registry

August 15, 2013

Completed
11 months until next milestone

First Posted

Study publicly available on registry

July 10, 2014

Completed
6 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 1, 2015

Completed
1.2 years until next milestone

Study Completion

Last participant's last visit for all outcomes

March 1, 2016

Completed
Last Updated

July 10, 2014

Status Verified

July 1, 2014

Enrollment Period

2.6 years

First QC Date

August 15, 2013

Last Update Submit

July 9, 2014

Conditions

Keywords

BurnSkin graftElasticitySkinPhysical therapy modalities

Outcome Measures

Primary Outcomes (1)

  • Elasticity of skin and scar

    The measurement of skin and scar elasticity will be measured by the used a noninvasive assessment equipment, Cutometer.

    3 years

Secondary Outcomes (2)

  • Erythema of skin and scar

    3 years

  • Fiber direction of skin and scar

    3 years

Study Arms (4)

Ultrasound group

EXPERIMENTAL

Therapeutic ultrasound, 3 MHz, continuous with intensity 1W/cm2 will be applied to the selected region (burn scar deep 2nd degree or 3rd degree, grafted) with exposure time of 2 minutes for each effective radiation area head (ERA), a total of 4 minutes of application in an area of 9X5 cm, and the application parameters with a matched control side of the patient, in a region with contralateral uninjured skin.

Device: ultrasound

Group paraffin

EXPERIMENTAL

Paraffin therapy is heated with thermostat own equipment, being applied to the selected region (burn scar deep 2nd degree or 3rd degree, grafted) and control (uninjured), with a length of 9X5 cm, at a temperature of 38 ° C with appropriate brush in layers (4 layers), remaining for 20 minutes. After the period of application of paraffin will be removed and discarded, with no reuse.

Device: paraffin

Ultrasound group + endermotherapy

EXPERIMENTAL

Therapeutic ultrasound, 3 MHz, continuous with intensity 1W/cm2 will be applied to the selected region (burn scar deep 2nd degree or 3rd degree, grafted) with exposure time of 2 minutes for each effective radiation area head (ERA), a total of 4 minutes of application in an area of 9X5 cm. The application of endermotherapy will be held shortly after the therapeutic ultrasound in a timely manner across the surface of the scar, for about 2 seconds per head area with a negative pressure between 100-200 mmHg, a total of 4 minutes application in an area of 9 x 5 cm. The same application parameters will be performed with one hand matched control patient, in a region with contralateral uninjured skin.

Device: ultrasoundDevice: endermotherapy

Group paraffin + endermotherapy

EXPERIMENTAL

Paraffin therapy is heated with thermostat own equipment, being applied to the selected region (burn scar deep 2nd degree or 3rd degree, grafted) and control (uninjured), with a length of 9X5 cm, at a temperature of 38 ° C with appropriate brush in layers (4 layers), remaining for 20 minutes. After the period of application of paraffin will be removed and discarded, with no reuse.The application of endermotherapy will be held shortly after the paraffin therapy in a timely manner across the surface of the scar, for about 2 seconds per head area with a negative pressure between 100-200 mmHg, a total of 4 minutes application in an area of 9 x 5 cm. The same application parameters will be performed with one hand matched control patient, in a region with contralateral uninjured skin.

Device: paraffinDevice: endermotherapy

Interventions

Ultrasound groupUltrasound group + endermotherapy
paraffinDEVICE
Group paraffinGroup paraffin + endermotherapy
Group paraffin + endermotherapyUltrasound group + endermotherapy

Eligibility Criteria

Age20 Years - 80 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Victims of deep second degree burns and third degree with a length of at least 1% of body surface area burned
  • Postoperative graft skin (4 and 6 months)
  • Anywhere in the body that has area to uninjured contralateral control
  • Good state of physical and mental health
  • Aged between 20 and 80 years
  • Both genders
  • Irrespective of race, class or social group

You may not qualify if:

  • Volunteers with illnesses or deformities that may interfere with evaluation and procedures

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of São Paulo

RibeirãoPreto, São Paulo, 14049-900, Brazil

RECRUITING

Related Links

MeSH Terms

Conditions

Burns

Interventions

UltrasonographyParaffin Embedding

Condition Hierarchy (Ancestors)

Wounds and Injuries

Intervention Hierarchy (Ancestors)

Diagnostic ImagingDiagnostic Techniques and ProceduresDiagnosisTissue EmbeddingTissue PreservationHistocytological Preparation TechniquesCytological TechniquesClinical Laboratory TechniquesHistological TechniquesInvestigative Techniques

Study Officials

  • Elaine Guirro, PhD

    University of Sao Paulo

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Elaine Guirro, PhD

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professor, PT, PhD

Study Record Dates

First Submitted

August 15, 2013

First Posted

July 10, 2014

Study Start

June 1, 2012

Primary Completion

January 1, 2015

Study Completion

March 1, 2016

Last Updated

July 10, 2014

Record last verified: 2014-07

Locations