Isometric Hand-Grip Exercise for Preventing Thrombosis and Occlusion of Midline Venous Catheters: A Randomized Controlled Trial
Effectiveness of Isometric Hand-grip Exercise in Preventing Thrombosis and Occlusion of Midline Peripheral Venous Catheters: a Randomized Controlled Trial.
1 other identifier
interventional
840
0 countries
N/A
Brief Summary
evaluate whether hand-grip ball exercises reduce thrombosis and occlusions of Midline catheters in hospitalized patients.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Jul 2026
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
June 11, 2026
CompletedFirst Posted
Study publicly available on registry
June 17, 2026
CompletedStudy Start
First participant enrolled
July 6, 2026
ExpectedPrimary Completion
Last participant's last visit for primary outcome
May 1, 2027
Study Completion
Last participant's last visit for all outcomes
September 1, 2027
June 17, 2026
June 1, 2026
10 months
June 11, 2026
June 11, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
To compare the effectiveness of a structured upper-limb exercise program versus usual care in reducing the incidence of Midline catheter-related thrombosis/occlusions in a population of hospitalized patients.
Incidence of Midline thrombosis (%) confirmed by ultrasound.
from enrollment until catether removal
Study Arms (2)
standard
NO INTERVENTIONusual care
handgrip
EXPERIMENTALuse of handgrip exercises in patients with midline catether
Interventions
Eligibility Criteria
You may qualify if:
- Midline catheter insertion for planned intravenous therapy lasting ≥ 7 days. Age between 18 and 70 years. Catheter inserted in the upper limb (forearm). Ability to understand and perform hand exercises with the limb bearing the venous catheter.
- Written informed consent.
You may not qualify if:
- Pre-existing superficial or deep venous thrombosis of the limb used for the Midline catheter.
- Limb injuries or amputations. Motor or neurological impairment of the hand. Life expectancy \< 7 days. Cognitive impairment/delirium. Medical contraindications to active upper-limb movement.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- PREVENTION
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- PI Degan Mario
Study Record Dates
First Submitted
June 11, 2026
First Posted
June 17, 2026
Study Start (Estimated)
July 6, 2026
Primary Completion (Estimated)
May 1, 2027
Study Completion (Estimated)
September 1, 2027
Last Updated
June 17, 2026
Record last verified: 2026-06
Data Sharing
- IPD Sharing
- Will not share