Impact of Comprehensive Rehabilitation Nursing Combined With Refined Airway Management and Nutrit… (NCT07025941) | Clinical Trial Compass
CompletedNot Applicable
Impact of Comprehensive Rehabilitation Nursing Combined With Refined Airway Management and Nutritional Support on Prognosis and Care Delivery Models in Critically Ill Patients
China101 participantsStarted 2023-06-02
Plain-language summary
This combined intervention protocol effectively improves the prognosis of critically ill patients and optimizes nursing management models
Who can participate
Age range
18 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Fulfillment of ICU admission standards with critical illness confirmed by attending physicians or senior specialists
* Age ≥ 18 years
* Stable vital signs:
Systolic blood pressure ≥ 90 mmHg and ≤ 180 mmHg
Heart rate ≤ 120 beats/min
Oxygen saturation (SpO₂) ≥ 85% under ≤ 60% fraction of inspired oxygen (FiO₂)
* Intact or tolerable gastrointestinal (GI) function for enteral nutrition
* Informed consent from both patients and families Exclusion Criteria:(1)
* Terminal malignancies
* Brain death
* Irreversible organ failure (e.g., end-stage cirrhosis, advanced heart failure)
* Comorbidities potentially confounding study outcomes
* Contraindications to interventions (e.g., laryngeal edema, complete intestinal obstruction)
* Pregnancy or lactation
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1This trial studied critically ill patients dealing with conditions like pulmonary infections, gastrointestinal bleeding, and acute kidney injury — does my specific situation match closely enough that the findings about rehabilitation nursing and airway management might be relevant to my care?
2Since this trial is already completed, has my care team had a chance to look at what it found about ICU length of stay, and could those results influence how my treatment or nursing plan is structured?
3The study combined three things at once — rehabilitation nursing, refined airway management, and nutritional support — so how would my doctor decide which of these elements, if any, make sense to prioritize in my individual case?
4Given that this was a nursing and care-delivery focused study rather than a drug trial, are these kinds of comprehensive rehabilitation approaches already being used in this hospital's ICU, or would asking for them require something special?
5Are there standard ICU care protocols my doctor would recommend first, and how does the combined approach tested in this trial compare to what I would receive under usual care here?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
ICU Length of Stay (LOS)
Timeframe: From randomization to ICU discharge, up to 60 days
Trial details
NCT IDNCT07025941
SponsorTaizhou Hospital of Traditional Chinese Medicine