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Electromuscular Stimulation Therapy as a Prophylactic Method to Reduce Thromboses Related to PICC Catheters in Patients Hospitalized in Critical Care Units. (ECOEMS)

I

Institut d'Investigació Biomèdica de Girona Dr. Josep Trueta

Status

Not yet enrolling

Conditions

Thrombosis; Catheter, Infusion Catheter (Vascular)

Treatments

Device: Protocol ECOEMS

Study type

Interventional

Funder types

Other

Identifiers

NCT06135857
2023.151

Details and patient eligibility

About

Introduction: The placement of a peripheral inserted central catheter (PICC) is a common practice in the hospital setting. However, despite all the advances reported, venous devices are not free of complications and catheter-related thrombosis (CRT), being one of the most prevalent. Electro muscular stimulation therapy can be a measure for the prevention of CRT. Objective: To know the efficacy of electro muscular stimulation therapy in patients hospitalized in critical care units to prevent venous thrombosis related to PICC catheters. Methodology: A multicenter Randomized Clinical Trial (RCT) will be carried out at the Dr. Josep Trueta University Hospital in Girona, Hospital del Mar in Barcelona, Althaia Foundation in Manresa. With a total of 68 patients with PICC catheters in critical care units, they will be randomly assigned to the intervention group (n=34) to whom, in addition to the usual protocolized care related to the vascular catheter, will be applied e Eco-EMS protocol, or the control group (n=34) to which only the usual protocolized care related to the vascular catheter was applied. Intervention: It will consist of the application of electrostimulation therapy five days a week, two daily sessions of 20 minutes in the intervention group. Both groups underwent five ultrasound examinations after the placement of the PICC to determine the appearance of CRT. Expected results: It is expected to observe that the application of the Eco-EMS protocol reduces thrombosis in the patients of the intervention group, compared to those of the control group.

Enrollment

68 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients admitted to the critical unit with a PICC whose insertion is done by the EIAV of the same hospital.
  • Patients between 18 and 80 years of age.
  • Treatments related to the device protocolized by the same hospital as the EIAV implanter.

Exclusion criteria

  • Patients who do not sign informed consent.
  • Patients with pacemakers and/or implantable automatic defibrillators.
  • Patients with epilepsy.
  • Removal of the device within the first 15 days after insertion.
  • Hospital discharge, transfer to another hospital or death lethalis during the duration of the study.
  • Displacement of the tip of the catheter outside the lower ⅓ of the superior vein cava during the study period.
  • Presence of lesions in the place where the electrodes must be placed to perform the electrostimulation therapy.
  • Non-compliance with catheter monitoring: Of the five ultrasound controls protocolized in the study, 80% were not complied with.

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

68 participants in 2 patient groups

Intervention group
Experimental group
Treatment:
Device: Protocol ECOEMS
Control group
No Intervention group

Trial contacts and locations

0

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Central trial contact

Ines Gerez Acevedo

Data sourced from clinicaltrials.gov

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