The Effectiveness of Stingless Bee Honey (Kelulut Honey) Versus Gel in Diabetic Wound Bed Preparation

Sponsor
Universiti Sains Malaysia (Other)
Overall Status
Recruiting
CT.gov ID
NCT04849143
Collaborator
(none)
76
1
2
21
3.6

Study Details

Study Description

Brief Summary

There has been no study yet on the effect of stingless bee honey (Kelulut honey) produced by Melipolini sp. in diabetic wound healing in Malaysia. Kelulut honey, apart from possessing similar pro-healing properties with other honey, is also found to have a better antioxidant capacity, anti-inflammatory, and free radical scavenging activity than Tualang honey. These effects are due to the much higher content of phenolic and flavonoid substances in Kelulut honey, the key bioactive factors promoting wound healing and preventing oxidative stress-related injury. Australian researchers have also recently discovered a novel source of the rare disaccharide trehalose in stingless bee's honey, which is highly anti-diabetic and antioxidating. This study aims to investigate the efficacy of honey against gel dressing for wound bed preparation among diabetic patients.

Condition or Disease Intervention/Treatment Phase
  • Other: Stingless bee honey ( Kelulut honey)
  • Other: Gel dressing
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
76 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Investigator, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
The Effectiveness of Stingless Bee Honey (Kelulut Honey) Dressing Versus Conventional Gel Dressing for Wound Bed Preparation in Diabetic Patients With Cavity Wounds: A Randomised Controlled Trial
Actual Study Start Date :
Sep 1, 2021
Anticipated Primary Completion Date :
Jun 1, 2023
Anticipated Study Completion Date :
Jun 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Honey dressing group

A thin layer of honey will be applied to the wounds

Other: Stingless bee honey ( Kelulut honey)
The honey will be acquired from Brainey Sdn Bhd, a company that provides stingless bee honey certified with Good Manufacturing Practice (GMP), ISO 22000, and Halal. As the honey used is not medical-grade honey, sterilization with 25kGy gamma-ray irradiation will be done for safety purposes to eradicate any potential life-threatening infection such as spores from Clostridium botulinum.

Active Comparator: Gel dressing group

A thin layer of gel will be applied to the wounds

Other: Gel dressing
Smith-Nephew's Intrasite gel

Outcome Measures

Primary Outcome Measures

  1. Size of granulation tissue [30 days]

    This will be calculated based on the surface area of granulation tissue traced and marked on the Opsite Flexigrid by indelible fine tip marker. The amount of small squares will calculated and this will represent the surface area. The change between baseline and at day 30 will be recorded as percentage.

  2. Wound size reduction [30 days]

    This will be calculated based on the surface area of the whole wound traced and marked on the Opsite Flexigrid by indelible fine tip marker. The amount of small squares will calculated and this will represent the surface area. The change between baseline and at day 30 will be recorded as percentage.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 70 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Male and female

  • Aged between 18-70 years old

  • Patient with full thickness cavity wound

  • Controlled diabetes mellitus (defined as: fasting blood glucose (FBG) < 10 mmol/L upon selection)

Exclusion Criteria:
  • Severely contaminated wound/infected

  • Patient with history of allergy to honey or stingless bee product

  • Patients who are immunocompromised or on chronic steroid use ( defined as use of steroid for more than 2 weeks)

  • Pregnancy

  • End stage renal failure (ESRF) patient

Contacts and Locations

Locations

Site City State Country Postal Code
1 Hospital Universiti Sains Malaysia Kota Bharu Kelantan Malaysia 16150

Sponsors and Collaborators

  • Universiti Sains Malaysia

Investigators

  • Principal Investigator: Mohamad Aizat Rosli, MB ChB, Universiti Sains Malaysia

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Mohamad Aizat Bin Rosli, Principal Investigator, Universiti Sains Malaysia
ClinicalTrials.gov Identifier:
NCT04849143
Other Study ID Numbers:
  • USM/JEPeM/21020186
First Posted:
Apr 19, 2021
Last Update Posted:
Aug 10, 2022
Last Verified:
Aug 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 10, 2022