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NCT07273669Active, not recruiting

Advanced Robotic Beds for the Early Rehabilitation of Cardiac Surgery Patients

Source: ClinicalTrials.gov · Last updated 9 Dec 2025

Brief summary (registry, in English)

The goal of this clinical trial is to evaluate whether LOLE.K, a new and specialized robotic bed, is effective in the rehabilitation of patients who have undergone surgery. The primary objectives of the trial are: * Efficacy of LOLE.K: Does the LOLE.K robotic bed improve early rehabilitation in patients who undergone cardiac surgery? * Impact on recovery: Does LOLE.K influence wound healing, muscle and neurological recovery, and psychological well-being? To address these questions, the researchers will compare the use of LOLE.K with standard physical therapy to determine whether the robotic bed results in better outcomes in post-operative rehabilitation.

Status (registry)
Active, not recruiting
Study type
Interventional
Enrollment
20 (estimated)
First submitted
26 Nov 2025
Start date
22 Sept 2025
Primary completion date
1 May 2026
Lead sponsor
University of Salerno
NCT number
NCT07273669

What you commit to

  • Study type: Interventional
  • Planned participants: 20
  • From 22 Sept 2025 to the primary completion date, 1 May 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Recent myocardial infarction (MI) with ST segment elevation (\< 72 hours)

Lab values

  • Left ventricular ejection fraction \< 30%
  • Clearance della creatinina \< 30 ml/min. Further exclusion criteria included bed rest orders, patients in a palliative care setting or with therapy limitations.
    • Restrictions due to the device were height outside the ranfe of 190cm, weight outside the range of 115kg, pacemakers, other electrical stimulators, or implanted medical pumps.

Age

  • Age \< 18 years old

Other

  • inability to provide informed consent, either verbally or in writing, or unwillingness to participate in systematic follow-up
  • Life expectancy \< 1 year

Who the study is looking for

  • patients undergoing aortic and mitral vale surgery
  • patients aged between 60 and 85

Age in the registry: 60 years to 85 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
AOU "San Giovanni di Dio e Ruggi d'Aragona"
Coordinator of this site? Confirm its status
SalernoItalyUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.