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

Study Locations

      • Sohag, Egypt, 82524
        • Recruiting
        • Sohag faculty of medicine

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
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.

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.

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