Effect of Double Tourniquet Technique on Ultrasonographic View of Forearm Veins
1 other identifier
observational
30
1 country
1
Brief Summary
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for all trials
Started Jan 2023
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
October 25, 2020
CompletedFirst Posted
Study publicly available on registry
November 3, 2020
CompletedStudy Start
First participant enrolled
January 15, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 1, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
July 1, 2024
CompletedSeptember 28, 2021
September 1, 2021
1.4 years
October 25, 2020
September 26, 2021
Conditions
Outcome Measures
Primary Outcomes (2)
Superficial forearm vein width and compressibility under ultrasonography
Ultrasonography is used to measure forearm superficial veins width and compressibility
1 minute after application of one proximal tourniquet
Superficial forearm vein width and compressibility under ultrasonography
Ultrasonography is used to measure forearm superficial veins width and compressibility
1 minute after application of two proximal tourniquet 1 cm apart
Interventions
Checking vein width snd copression using US
Eligibility Criteria
Community sample
You may qualify if:
- Healthy volunteers aged 18-60 years will participate in the study
You may not qualify if:
- patients with dialysis shunts, previous mastectomy on the examined side, fracture , skin lesion , burn or edema on the examined side
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Sohag faculty of medicine
Sohag, 82524, Egypt
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Officials
- 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
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- Lecturer of anesthesia and ICU sohag university
Study Record Dates
First Submitted
October 25, 2020
First Posted
November 3, 2020
Study Start
January 15, 2023
Primary Completion
June 1, 2024
Study Completion
July 1, 2024
Last Updated
September 28, 2021
Record last verified: 2021-09