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Skeletal Muscle Mass on Prognosis and Recovery in Clinical Trial

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National Taiwan University

Status

Invitation-only

Conditions

Out of Hospital Cardiac Arrest
Inhospital Cardiac Arrest

Treatments

Behavioral: Enhanced Rehabilitation Program

Study type

Interventional

Funder types

Other

Identifiers

NCT07034170
202501085RIND

Details and patient eligibility

About

The objective of this research project is to develop an automated muscle mass measurement system based on computed tomography (CT) images using deep learning and artificial intelligence, and to construct a prognostic prediction model for patients who have experienced cardiac arrest and undergone resuscitation. The model will be validated using multicenter registry data and medical imaging. Furthermore, a clinical trial involving core muscle rehabilitation for post-resuscitation patients will be conducted to evaluate both short-term and long-term outcomes, aiming to comprehensively understand the impact of muscle mass on the prognosis of patients after cardiac arrest.

Enrollment

90 estimated patients

Sex

All

Ages

18 to 99 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Non-traumatic adult patients who experienced sudden cardiac arrest
  • Achieved sustained return of spontaneous circulation (ROSC) for more than five minutes following successful resuscitation
  • Admitted to the ICU
  • Survived beyond 72 hours without successful weaning from mechanical ventilation

Exclusion criteria

  • Age under 18 years
  • Pregnancy
  • Expected to be weaned from mechanical ventilation within 48 hours
  • Terminal-stage cancer or unwillingness to receive aggressive treatment
  • Unavailability of ICU care due to overcrowding in the emergency intensive care unit
  • Refusal to participate in the study by the patient or family members
  • Presence of an implanted pacemaker or defibrillator
  • Open wounds, severe edema, or deep vein thrombosis in the lower limbs
  • Pre-arrest status limited to wheelchair use or bedridden, unable to ambulate

Trial design

Primary purpose

Supportive Care

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

90 participants in 2 patient groups

control group
No Intervention group
Intervention Group
Experimental group
Treatment:
Behavioral: Enhanced Rehabilitation Program

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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