Condition: Critical Care, Intensive Care · Sponsor: Bakirkoy Dr. Sadi Konuk Research and Training Hospital
Dear participant Participants's patient, who is participants's first-degree relative, who is connected to a ventilator in the intensive care unit, unconscious and not authorized to give informed consent, has been invited to participate in the study titled 'Does transcutaneous phrenic nerve stimulation prevent diaphragm atrophy? In order to strengthen this muscle and prevent loss of function, investigator provide electrical stimulation between the rib cage and abdomen through the skin with the tens device, causing the muscle to contract and enabling our patient to leave the respirator early. Investigator aimed to investigate the protective effect of the tens device on the diaphragm by evaluating the diaphragm muscle with the ultrasonography device during the period when it is connected to the respirator. For this reason, the diaphragm will be contracted by giving electrical stimulation three times a day for 30 minutes with the tens device for 5 days during the period when participants's patient is connected to the respirator, and intermittent diaphragm ultrasound will be evaluated. Participants or participants's legal guardian are asked to approve the use of participants's medical records during participants's treatment in the intensive care unit, provided that participants's personal information is kept confidential. Participants will not incur any financial burden by participating in the study and participants will not receive any additional payment. Participants are fre…
This description comes directly from the study's public registry record.
Safiye Tuba Kaplan · +9 · sipahituba79@gmail.com
Always discuss trial participation with your own doctor first.
| Dr.SadiKonuk EAH | Istanbul, Bakirkoy, Turkey (Türkiye) | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06897774