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Effect of aloe vera gels on pain and recovery of surface burn wound grade II

Comparison the effect of Aloevera Gels and nitroforazon2% on pain and recovery of surface burn wound grade II

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014113020151N1
Enrollment
30
Registered
2014-12-14
Start date
2014-12-03
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

burn. Burn of second degree, body region unspecified

Interventions

In the control area for 3 weeks wound daily washed whit normal salin 0.9% and used nitroforazon 2% on the burned wound that the amount ointment is determinate by the doctor and they are reviewed in
Placebo

Sponsors

Tehran University of Medical sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: ( Inclusion criteria:Patients whit grade 2 burns wounds ; Burns of less than 20% without infection ; The doctor has prescribed for the treatment of nitroforazon2% ; according to the doctor don’t require hospitalization and out patient treatment done, underlying diseases such as Diabetes and Immune system such as Cancer , Aids and severe skin allergies and skin problem ; Don’t used of smoking and alcohol ; Willingness to participate in research and to be able to answer questions ; Burns caused by heat source or hot liquids ; From burn time up to admission to hospital for further dressing petition hold more than 6 hours ; burn wound is not infected with any of the contaminants of any substance other than potable is not used on wounds. And Exclusion criteria:severe allergic skin to aleo vera gels skin ; causing infection in of the areas burned such as: There is swelling in the area burned associated induration inflammation of the edges of the wound, change color burned wound to burnt red, brown, purple or black, purulent discharge, stink, green and abundant ; fever during course of treatment )

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Recovery. Timepoint: in weeks 1 and 2 and 3 after firsti dressing. Method of measurement: bots-jons tool.;Pain. Timepoint: befor dressing and 24 and 48 and 72 hours after dressing. Method of measurement: used from Visual Analouge Scale (vas).

Secondary

MeasureTime frame
Infection. Timepoint: Check daily During the intervention. Method of measurement: signs incidence such as :there is swelling in the area burned whit associated Induration inflamation of the edges wound change color wound brunt to dark, red, brown, purple or black, purulent discharge, stink, green and abandunt and fever.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactParichehr Sabaghzadeh Irani

Tehran University Medical Sciences School of Nursing and Midwifery

fnmsite@tums.ac.ir+98 66927171

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026