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NCT Number: NCT06814405

Safety and Feasibility of a Multidisciplinary Programme of Integrated Hospital-home Management With Early Discharge of Patients With Haematological Malignancies Undergoing High-dose Chemotherapy in Hospital

Patients undergoing particular intensive and (sub)myeloablative chemotherapy regimens with subsequent autologous stem cell transplant currently have a relatively low rate of therapy-related complications, both infectious and non-infectious (organ damage), and can therefore benefit from a specific multidisciplinary care programme at home. In this clinical context, early discharge and domicile of the patient after therapy provided in a hospital setting may represent a procedure designed to better intercept the patient's personal needs. In addition, it may make it possible to increase the limited availability of beds in the face of the progressive increase in demand, allowing the provision of hospital therapies to a higher number of patients with a consequent reduction in pre-hospital waiting times.

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

IRCCS-AOU di Bologna

Bologna, 40138, Italy

Location status: Recruiting

Location contact

Pier Luigi Zinzani, MD

CONTACT

[email protected]

+39 0512143680

Pier Luigi Zinzani, MD

PRINCIPAL_INVESTIGATOR

About this study

Patients undergoing particular intensive and (sub)myeloablative chemotherapy regimes with subsequent autologous stem cell transplant currently have a relatively modest rate of therapy-related complications, of infectious and non-infectious (organ damage), relatively modest, thus being able to benefit of a specific multidisciplinary care programme at home. In this clinical context, the early discharge and domicile of the patient after therapy provided in hospital regimen may represent a procedure designed to better intercept the patient's patient's personal needs. In addition, it may make it possible to increase the limited availability of beds against the progressive increase in demand, allowing the provision of hospital treatment to a higher number of patients with a consequent reduction in pre-admission waiting times. The primary objective of the study is to assess the safety and feasibility of the model of early discharge with home continuation of the care pathway of patients haematological patients undergoing high-dose chemotherapy with/without autologous stem cell transplant.

The secondary objectives are as follows:

  • Assessment of the patient's quality of life;
  • Evaluation of the impact of the use of innovative remote monitoring technologies;
  • Assessment of the optimisation of in-patient places;
  • Evaluation of the economic impact.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Diagnosis of haematological malignancy undergoing high-dose chemotherapy (sub- or myeloablative)
  • Age between 18-75 years
  • WHO Performance Status < 2 or Karnofsky ≥ 60%
  • Adequate organ function:
  • FE≥ 50% and absence of significant electrocardiographic changes
  • eVFG > 40 ml/min and/or creatinine ≤ 1.6 mg/dl (CPK-EPI formula)
  • total bilirubin ≤ 3 mg/ml
  • AST/ALT ≤ 5 ULN
  • SpO2 ≥ 94%
  • Reinfusion ≥ 2x106 CD34+/Kg
  • Presence of a 24-hour SARS-COV-2 vaccinated caregiver
  • Home < 45 minutes' drive from hospital
  • Informed consent obtained

Exclusion criteria

  • Diagnosis of haematological malignancy at onset or in progression
  • Significant cardiovascular disease: heart failure NYHA class 3 or 4, uncontrolled angina, history of myocardial infarction, unstable angina or stroke in the previous 6 months, uncontrolled hypertension, significant arrhythmias not controlled by medication

Treatment and study plan

Home patient management

Procedure

with support therapy, Granulocyte growth factor, blood transfusion

Hospital patient management

Other

all procedures and exams needed

Primary outcomes

  1. Number of participants with treatment-related adverse events

    Time frame: through the duration of study, an average of 2 years

    safety of the early discharge model with home continuation of the care pathway of haematological patients undergoing high-dose chemotherapy with/without autologous stem cell transplant

  2. Number of participants in which will be feasible the early discarge mode

    Time frame: through the duration of study, an average of 2 years

    feasibility of the early discharge model with home continuation of the care pathway of haematological patients undergoing high-dose chemotherapy with/without autologous stem cell transplant

Secondary outcomes

  1. questionnaire patient's quality of life FACT-An (Functional Assessment of Cancer Therapy) (V. 4, scale 0-4)

    Time frame: through the duration of study, an average of 2 years

    Assessment of the patient's quality of life with questionnaire FACT-An(Functional Assessment of Cancer Therapy) (V. 4, scale 0-4) at early discharge and recovery hematology

  2. Median length of stay with early discharge (outpatient)/median length of hospitalization without early discharge (inpatient) of patients who were enrolled but, for reasons various, were not discharged early;

    Time frame: through the duration of study, an average of 2 years

    Median length of stay with early discharge (outpatient)/median length of hospitalization without early discharge (inpatient) of patients who were enrolled but, for reasons various, were not discharged early;

  3. rate of optimisation of in-patient places

    Time frame: through the duration of study, an average of 2 years

    Assessment of optimisation of in-patient places

  4. Rate of Economic Impact

    Time frame: through the duration of study, an average of 2 years

    Economic Impact Assessment

Study contacts

Contact information is provided by the study sponsor or research team.

Pier Luigi Zinzani, MD

CONTACT

[email protected]

+39 0512143680

Sponsors and collaborators

Lead sponsor

IRCCS Azienda Ospedaliero-Universitaria di Bologna

Other

Registry information

Acronym: AMICO

Important dates

Study start
2023
Primary completion
2025
Study completion
2025
First posted
Feb 7, 2025
Registry last updated
Feb 7, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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