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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04277182
Other study ID # 2019-048
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 1, 2020
Est. completion date September 28, 2020

Study information

Verified date August 2022
Source Izmir Katip Celebi University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This experimental study will be carried out at Ege University Laboratory Animals Application and Research Center to identify the efficacy of 10% propolis and 15% propolis on wound healing in a second-degree superficial burn wound. In the study, 36 adult (8-12 week old) Wistar-Albino rats with a weight of 200-300 grams will be used in each group. Each group will include 6 rats. Stratified randomization will be used to randomize rats according to their gender and weight. After randomization, a burnt area will be created on the back of the rats and dressings will be made every day. Following the creation of the burn, biopsy samples will be taken on the 3rd, 7th, 14th and 21st days and at the light microscopic level; bulla, erythema, oedema, burn depth, inflammatory cell infiltration, necrosis, ulceration, angiogenesis, neovascularization, fibroblast proliferation, collagenization, epithelization, fibrosis, the number of hair follicles and damage to the skin attachments. In the immunohistochemical examination of biopsy samples, samples will be taken for the evaluation of superoxide dismutase, malondialdehyde, myeloperoxidase in the evaluation of the tumour necrosis factor-alpha, interleukin-1β and oxidative stress in the EBB period in order to evaluate the acute phase reactants. Fungal and gram staining will be done in order to determine the pathogen reproduction in biopsy samples taken on the 3rd and 7th day. Masson trichrome in order to detect fibrosis in biopsy samples taken on the 14th and 21st day; Hydroxyproline examination will be examined in order to evaluate collagen formation.


Recruitment information / eligibility

Status Completed
Enrollment 36
Est. completion date September 28, 2020
Est. primary completion date September 28, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 8 Weeks to 12 Weeks
Eligibility Inclusion Criteria: - adult (8-12 weeks) - 200-300 grams - Wistar-Albino rat - with 4 second-degree superficial contact burn are at its back. Exclusion Criteria: - the death of the rat in the research process

Study Design


Related Conditions & MeSH terms


Intervention

Biological:
burn wound dressing
st. group: It will be considered as a control group and rats will not be treated. nd. group: Vehicle group, Propolis vehicle will be applied topically to rats for 21 days. rd group: Silver Sulfadiazine group, 1% Silver Sulfadiazine will be applied topically to rats for 21 days. th. group: Nitrafurozon group, 0.2% Nitrafurozon will be applied topically for 21 days. th. group: 10% Propolis group, 10% Propolis will be applied topically for 21 days. th. group: 15% Propolis group, 15% Propolis will be applied topically for 21 days.

Locations

Country Name City State
Turkey Ege University I?zmi?r

Sponsors (1)

Lead Sponsor Collaborator
Izmir Katip Celebi University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary wound size photos will be taken every day to determine the wound size 21 days
Primary bulla examination of the skin at the light microscopic level. Bulla will be considered as present or absent. 3rd day of the research
Primary bulla examination of the skin at the light microscopic level. Bulla will be considered as present or absent. 7th day of the research
Primary bulla examination of the skin at the light microscopic level. Bulla will be considered as present or absent. 14th day of the research
Primary bulla examination of the skin at the light microscopic level. Erythemawill be considered as present or absent. 21st day day of the research
Primary edema examination of the skin at the light microscopic level. Edema will be considered as present or absent. 3rd day of the research
Primary edema examination of the skin at the light microscopic level. Edema will be considered as present or absent. 7th day of the research
Primary edema examination of the skin at the light microscopic level. Edema will be considered as present or absent. 14th day of the research
Primary edema examination of the skin at the light microscopic level. Edema will be considered as present or absent. 21st day of the research
Primary inflammatory cell infiltration examination of the skin at the light microscopic level. Inflammatory cell infiltration will be considered as present or absent. 3rd day of the research
Primary inflammatory cell infiltration examination of the skin at the light microscopic level. Inflammatory cell infiltration will be considered as present or absent. 7th day of the research
Primary inflammatory cell infiltration examination of the skin at the light microscopic level. Inflammatory cell infiltration will be considered as present or absent. 14th day of the research
Primary inflammatory cell infiltration examination of the skin at the light microscopic level. Inflammatory cell infiltration will be considered as present or absent. 21st day of the research
Primary necrosis examination of the skin at the light microscopic level. Necrosis will be considered as present or absent. 3rd day of the research
Primary necrosis examination of the skin at the light microscopic level. Necrosis will be considered as present or absent. 7th day of the research
Primary necrosis examination of the skin at the light microscopic level. Necrosis will be considered as present or absent. 14th day of the research
Primary necrosis examination of the skin at the light microscopic level. Necrosis will be considered as present or absent. 21st day of the research
Primary ulceration examination of the skin at the light microscopic level. Ulceration will be considered as present or absent. 3rd day of the research
Primary ulceration examination of the skin at the light microscopic level. Ulceration will be considered as present or absent. 7th day of the research
Primary ulceration examination of the skin at the light microscopic level. Ulceration will be considered as present or absent. 14th day of the research
Primary ulceration examination of the skin at the light microscopic level. Ulceration will be considered as present or absent. 21st day of the research
Primary angiogenesis examination of the skin at the light microscopic level. Angiogenesis will be considered as present or absent. 3rd day of the research
Primary angiogenesis examination of the skin at the light microscopic level. Angiogenesis will be considered as present or absent. 7th day of the research
Primary angiogenesis examination of the skin at the light microscopic level. Angiogenesis will be considered as present or absent. 14th day of the research
Primary angiogenesis examination of the skin at the light microscopic level. Angiogenesis will be considered as present or absent. 21st day of the research
Primary fibroblast proliferation examination of the skin at the light microscopic level. Fibroblast proliferation will be considered as present or absent. 3rd day of the research
Primary fibroblast proliferation examination of the skin at the light microscopic level. Fibroblast proliferation will be considered as present or absent. 7th day of the research
Primary fibroblast proliferation examination of the skin at the light microscopic level. Fibroblast proliferation will be considered as present or absent. 14th day of the research
Primary fibroblast proliferation examination of the skin at the light microscopic level. Fibroblast proliferation will be considered as present or absent. 21st day of the research
Primary epithelization examination of the skin at the light microscopic level. Epithelization will be considered as present or absent. 3rd day of the research
Primary epithelization examination of the skin at the light microscopic level. Epithelization will be considered as present or absent. 7th day of the research
Primary epithelization examination of the skin at the light microscopic level. Epithelization will be considered as present or absent. 14th day of the research
Primary epithelization examination of the skin at the light microscopic level. Epithelization will be considered as present or absent. 21st day of the research
Primary collagenization examination of the skin at the light microscopic level. Collagenization will be considered as present or absent. 3rd day of the research
Primary collagenization examination of the skin at the light microscopic level. Collagenization will be considered as present or absent. 7th day of the research
Primary collagenization examination of the skin at the light microscopic level. Collagenization will be considered as present or absent. 14th day of the research
Primary collagenization examination of the skin at the light microscopic level. Collagenization will be considered as present or absent. 21st day of the research
Primary microorganism colonization examination of the skin at the light microscopic level. Colonization will be considered as present or absent. 3rd day of the research
Primary microorganism colonization examination of the skin at the light microscopic level. Colonization will be considered as present or absent. 7th day of the research
Primary microorganism colonization examination of the skin at the light microscopic level. Colonization will be considered as present or absent. 14th day of the research
Primary microorganism colonization examination of the skin at the light microscopic level. Colonization will be considered as present or absent. 21st day of the research
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