- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05326022
Microcurrent Therapy and Low-Level Laser Therapy on Wound Healing
April 6, 2022 updated by: Nehad Ahmed Youness Abo-zaid
Microcurrent Therapy Versus Low-Level Laser Therapy on Post-surgical Wound Healing
The study aiming to compare between the Microcurrent and Low-Level Laser Therapy on wound healing
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Detailed Description
The study designed to compare between the Microcurrent and Low-Level Laser Therapy on wound healing
Study Type
Interventional
Enrollment (Anticipated)
90
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Nehad A. Abo-Zaid, PhD
- Phone Number: +201223265216
- Email: dr.nehadahmed@svu.edu.eg
Study Contact Backup
- Name: Mohammed E. Ali, PhD
- Phone Number: +201011212425
- Email: m.essam@svu.edu.eg
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
10 years to 50 years (ADULT, CHILD)
Accepts Healthy Volunteers
No
Genders Eligible for Study
Male
Description
Inclusion Criteria:
- patient recently undergo appendectomy
Exclusion Criteria:
- patient with neurological disorders
- patient with metabolic disorders
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: TREATMENT
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: DOUBLE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
EXPERIMENTAL: medical therapy group
formed of 20 patients to whom ordinary medical therapy as the pervious groups and placebo shame laser had been applied.
|
Medical therapy
|
|
EXPERIMENTAL: medical therapy and Microcurrent group
formed of 20 patients to whom the microcurrent therapy had been applied with ordinary medical therapy.
|
Medical therapy
Microcurrent therapy
|
|
EXPERIMENTAL: medical therapy and Low-Level Laser Therapy group
formed of 20 patients to whom the Low Level Laser Therapy had been applied with ordinary medical therapy.
|
Medical therapy
Laser therapy
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
levels of matrix metalloproteinases
Time Frame: assessed at day 3 post operative
|
analyze by Enzyme-linked immunosorbent assay
|
assessed at day 3 post operative
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
levels of matrix metalloproteinases
Time Frame: assessed at day 30 post operative
|
analyze by Enzyme-linked immunosorbent assay
|
assessed at day 30 post operative
|
|
the tissue inhibitors of metalloproteinases
Time Frame: assessed at day 3 post operative
|
analyze by Enzyme-linked immunosorbent assay
|
assessed at day 3 post operative
|
|
the tissue inhibitors of metalloproteinases
Time Frame: assessed at day 30 post operative
|
analyze by Enzyme-linked immunosorbent assay
|
assessed at day 30 post operative
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Nehad A. Abo-zaid, PHD, South Valley University
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (ANTICIPATED)
April 28, 2022
Primary Completion (ANTICIPATED)
September 30, 2022
Study Completion (ANTICIPATED)
October 30, 2022
Study Registration Dates
First Submitted
March 23, 2022
First Submitted That Met QC Criteria
April 6, 2022
First Posted (ACTUAL)
April 13, 2022
Study Record Updates
Last Update Posted (ACTUAL)
April 13, 2022
Last Update Submitted That Met QC Criteria
April 6, 2022
Last Verified
April 1, 2022
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- P.T.REC/012/002599
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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