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Evaluation of an Organized Consultation "Return Home" of Patients With a Cancer (CREDO)

I

Institut Claudius Regaud

Status

Completed

Conditions

METASTATIC CANCER

Treatments

Other: CREDO standard of care
Other: current standard of care

Study type

Interventional

Funder types

Other

Identifiers

NCT02857400
16GENE11

Details and patient eligibility

About

Prospective, open label, randomized and multicentric study evaluating the efficacy of an organized consultation "return home" compared to a current standard of care in patient hospitalized due to metastatic solid tumor cancer.

Subject will be randomized (1:1) as described below :

• Arm A (standard) : current standard of care ; connection documentation faxed to GP ( General practitioner) on the day of patient's discharge Arm B (experimental) : CREDO standard of care, organized consultation "return home" between patient, GP DESC (diploma of complementary specialized study) and patient's referent GP

Enrollment

667 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Age > or = 18 years old
  2. Subject hospitalized in an oncology dedicated center for administration of the first chemotherapy cycle.
  3. Subject with metastatic solid tumor whatever the organ
  4. subject planned to be discharged home after chemotherapy administration
  5. Affiliated to the French social security system.
  6. Subjects must provide written informed consent prior to any study-specific procedure or assessment

Exclusion criteria

  1. Subject included in another trial evaluating the pathways care
  2. Pregnant or breastfeedings women
  3. Subject law protected

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

667 participants in 2 patient groups

Arm A (standard)
Other group
Treatment:
Other: current standard of care
Arm B (experimental)
Experimental group
Treatment:
Other: CREDO standard of care

Trial contacts and locations

3

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Data sourced from clinicaltrials.gov

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