Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
30 participants
INTERVENTIONAL
2022-11-09
2024-03-01
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
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Group 1
Group 1 received topical application of Bee Venom gel, 3 times per week
group 1 received topical Bee venom gel
Group 1 received a topical application of Bee Venom gel, 3 times per weeks. The wound dressing changed day after day and was cleaned every time with normal saline.
group 2
Group 1 received phonophoresis of Bee Venom gel using low intensity ultrasound, 3 times per week
Group 2: Phonophoresis of Bee Venom gel
group 2 received phonophoresis of Bee Venom gel using low frequency ultrasound, 3 times per weeks
Interventions
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group 1 received topical Bee venom gel
Group 1 received a topical application of Bee Venom gel, 3 times per weeks. The wound dressing changed day after day and was cleaned every time with normal saline.
Group 2: Phonophoresis of Bee Venom gel
group 2 received phonophoresis of Bee Venom gel using low frequency ultrasound, 3 times per weeks
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* Patients with renal, and
* Patients with hepatic diseases and
* Diabetic patients. Additionally,
* Patients with immunosuppressive diseases,
* Patients with HIV, and
* Anemia Patients
40 Years
60 Years
ALL
No
Sponsors
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Badr University
OTHER
Responsible Party
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Reham Alaa
lecturer of physical therapy
Principal Investigators
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Ashraf Hassan, professor
Role: STUDY_DIRECTOR
Badr University in Cairo
Locations
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Badr University in Cairo
Cairo, , Egypt
Countries
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Other Identifiers
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BUC-IACUC-221109-6
Identifier Type: -
Identifier Source: org_study_id
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