- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04613011
Effect of Double Tourniquet Technique on Ultrasonographic View of Forearm Veins
September 26, 2021 updated by: Bahaa Mohammed Refaie
Effect of Double Tourniquet Technique on Width and Compressibility of Superficial Veins of Forearm
Vein compressibility will be assessed after light pressure applied with the ultrasound probe.
Vein compressibility will be graded as 3 (100% compressed), 2 (50-100 compressed), and 1 (less than 50% compressed).
After baseline measurements were taken, a proximal tourniquet will be applied to mid-arm.
Repeated measurements of depth, width, and compressibility will be taken one minute after the tourniquet was applied.
Same measurements will be repeated again with second tourniquet applied 1 cm distal to the first tournique.
Study Overview
Status
Recruiting
Intervention / Treatment
Study Type
Observational
Enrollment (Anticipated)
30
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: Bahaa Mohammed Refaie, MD
- Phone Number: 0201026887257
- Email: bahaarefaay@med.sohag.edu.gov.eg
Study Locations
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Sohag, Egypt, 82524
- Recruiting
- Sohag faculty of medicine
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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
18 years to 60 years (Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
Community sample
Description
Inclusion Criteria:
- Healthy volunteers aged 18-60 years will participate in the study
Exclusion Criteria:
- patients with dialysis shunts, previous mastectomy on the examined side, fracture , skin lesion , burn or edema on the examined side
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Superficial forearm vein width and compressibility under ultrasonography
Time Frame: 1 minute after application of one proximal tourniquet
|
Ultrasonography is used to measure forearm superficial veins width and compressibility
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1 minute after application of one proximal tourniquet
|
|
Superficial forearm vein width and compressibility under ultrasonography
Time Frame: 1 minute after application of two proximal tourniquet 1 cm apart
|
Ultrasonography is used to measure forearm superficial veins width and compressibility
|
1 minute after application of two proximal tourniquet 1 cm apart
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Chair: Bahaa M Refaie, MD, Lecturer of anesthesia and ICU sohag university
- Study Director: Hosam eldeen M Marie, MD, Consultant of anesthesia and ICU at Elhelal insurance hospital sohag
- Principal Investigator: Mohammed A Ibrahim, MD, Lecturer of anesthesia and ICU sohag university
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)
January 15, 2023
Primary Completion (Anticipated)
June 1, 2024
Study Completion (Anticipated)
July 1, 2024
Study Registration Dates
First Submitted
October 25, 2020
First Submitted That Met QC Criteria
October 27, 2020
First Posted (Actual)
November 3, 2020
Study Record Updates
Last Update Posted (Actual)
September 28, 2021
Last Update Submitted That Met QC Criteria
September 26, 2021
Last Verified
September 1, 2021
More Information
Terms related to this study
Other Study ID Numbers
- 1900
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
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.