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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04785508
Other study ID # 2672
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date February 15, 2021
Est. completion date July 2024

Study information

Verified date January 2024
Source Fondazione Policlinico Universitario Agostino Gemelli IRCCS
Contact Maria Enrica Antoniucci, MD
Phone + 393335492584
Email mariaenrica.antoniucci@policlinicogemelli.it
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study aims to verify the efficacy of the decompression technique of neuromuscular taping on cardiac surgery patients in whom edema of the upper limbs occurs due to post-operative water overload.


Recruitment information / eligibility

Status Recruiting
Enrollment 10
Est. completion date July 2024
Est. primary completion date June 2024
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - Cardiac surgery patients with postoperative edema of the upper limbs due to water overload Exclusion Criteria: - absence of edema, - previous mastectomy and lymphadenectomy, - surgery or fractures or infection of the upper limb, - previous or current deep vein thrombosis.

Study Design


Related Conditions & MeSH terms


Intervention

Device:
neuromuscolar tape
neuromuscalar tape application in decompression technique (hand and arm)
Behavioral:
antigravity arm position
antigravity arm position

Locations

Country Name City State
Italy Maria Enrica Antoniucci Roma

Sponsors (1)

Lead Sponsor Collaborator
Fondazione Policlinico Universitario Agostino Gemelli IRCCS

Country where clinical trial is conducted

Italy, 

Outcome

Type Measure Description Time frame Safety issue
Primary circumference's change of index finger, metacarpus, wrist, mid forearm, elbow and upper arm measure tissue edema change by circumference change in specific site of the limb ( index finger, metacarpus, wrist, mid forearm, elbow and upper arm) measure in millimeter on first postoperative day: before application of tape; and then, every day for the first 3 days, after tape removing, and before the new application.
Secondary measurement of the intensity of pain measurement of the intensity of pain during mobilization of fingers, wrist and arm using a VAS scale( 0 is no pain and 10 is the worst possible pain) Measure every day for the 3 days of treatment, before application of tape
Secondary movement ability of wrist, hand and arm measure angle variation in pronosupination and flexion extension, ulnar and radial deviation of the wrist with articular goniometer measure every day for the 3 days of treatment, before application of tape
Secondary muscle strength measure measurement of the handheld gripping force by means of a dynamometer measure every day for the 3 days of treatment, before application of tape