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Tackling Pressure Ulcer Via Bee Venom Phonophoresis

Not Applicable
Completed
Conditions
Pressure Ulcers
Phonophoresis
Bee Venom
Interventions
Other: group 1 received topical Bee venom gel
Registration Number
NCT06374563
Lead Sponsor
Badr University
Brief Summary

This study aimed to investigate the efficiency of topical Bee Venom gel versus phonophoresis of Bee Venom gel to accelerate healing of chronic pressure ulcer

Detailed Description

In this study, the Bee Venom gel was prepared in a gel formula. Patients with chronic pressure ulcers were enrolled randomly into two different groups. Group 1 received a topical application of Bee Venom gel, 3 times per weeks. While group 2 received phonophoresis of Bee Venom gel using low frequency ultrasound, 3 times per week. The treatment lasted for 8 consecutive weeks. The Image J Software is used to measure the wound surface area before and after treatment.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
30
Inclusion Criteria
  • Patients with stage II and III chronic neuropathic ulcers.
Exclusion Criteria
  • Patients with chronic cardiac,
  • Patients with renal, and
  • Patients with hepatic diseases and
  • Diabetic patients. Additionally,
  • Patients with immunosuppressive diseases,
  • Patients with HIV, and
  • Anemia Patients

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Group 1group 1 received topical Bee venom gelGroup 1 received topical application of Bee Venom gel, 3 times per week
Primary Outcome Measures
NameTimeMethod
wound surface area wound surface areaBefore starting treatment and after 8 weeks of treatment

ImageJ Software was used to measure the wound size

wound volumeBefore starting treatment and after 8 weeks of treatment

wound volume was measured through the volumetric measurement method using a syringe filled with saline

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Badr University in Cairo

🇪🇬

Cairo, Egypt

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