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Effect of Double Tourniquet Technique on Ultrasonographic View of Forearm Veins

Effect of Double Tourniquet Technique on Width and Compressibility of Superficial Veins of Forearm

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04613011
Enrollment
30
Registered
2020-11-03
Start date
2023-01-15
Completion date
2024-07-31
Last updated
2021-09-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Superficial Forearm Veins Compressibility and Width

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.

Interventions

DEVICEUltrasound

Checking vein width snd copression using US

Sponsors

Bahaa Mohammed Refaie
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
Superficial forearm vein width and compressibility under ultrasonography1 minute after application of one proximal tourniquetUltrasonography is used to measure forearm superficial veins width and compressibility

Countries

Egypt

Contacts

Primary ContactBahaa Mohammed Refaie, MD
bahaarefaay@med.sohag.edu.gov.eg0201026887257

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026