Track this trial free. DataLookout checks ClinicalTrials.gov daily and emails you which fields changed on NCT05723185 (status, enrollment, completion dates, endpoints, sites) when this record is updated. Free accounts track up to 5 trials.

Track this trial

Primary Care-Hospital Embedding: a Prospective, Multicentric, Observational Study

Study acronym: PRIME
StatusActive, Not Recruiting
PhaseNot specified
Started
View on ClinicalTrials.gov ↗

Record History

  1. Minor Trial status: Recruiting to Active, Not Recruiting
    • Primary completion date changed from estimate of Jan 31, 2024 to Aug 31, 2023
    • Study completion date: Jan 31, 2024 to Dec 31, 2025
    • Site details revised
    v3
  2. Minor Start date changed from estimate of Feb 6, 2023 to Feb 13, 2023v2
  3. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
8,786 trials monitored
See 412 trials at risk
5,087 trials monitored
See 222 trials at risk
1,995 trials monitored
See 111 trials at risk
and 2 more diseases
This is a multicentric, prospective, observational study with two cohorts and adjunctive procedure. It aims at collecting and analyzing data about the function of an innovative hospital-territory integration health service for the management of patients with intermediate urgency, or emergency department "white codes." This service, activated in the participating centers, will be provided in two alternative modalities, one so-called "dual specialty" (cardiology and diabetes specialist outpatient clinic) and a second one more focused on the figure of the specialist in Internal Medicine. The investigators will monitor the population treated in these centers (presenting complaint, medical history, clinical-radiological data, performed therapies and overall health path) and the degree of satisfaction of the General Practitioners who sent their patients there and the degree of satisfaction of the patients themselves. The data collected will also be used to evaluate the effectiveness of the outpatient clinics in terms of reducing improper admissions to the Emergency Departments and hospitalizations. The two modes of service delivery will be compared. This is an 18-month study, sponsored by our Scientific Directorate and carried out on a nonprofit basis. The study will enroll 246 patients and 30 healthy volunteer General Practitioners. The clinical trial will be conducted in accordance with Good Clinical Practice standards.
Trial Details
NCT Number NCT05723185
Lead Sponsor Rovere Querini Patrizia
Collaborators: ASST Fatebenefratelli Sacco, ASST Grande Ospedale Metropolitano Niguarda
Conditions
(from sponsor)
Heart Failure, Chronic Obstructive Pulmonary Disease, Diabetes Mellitus, Pneumonia, Urinary Tract Infections, Fever of Unknown Origin, Deep Vein Thrombosis, Hypertension
Related terms Diabetes Mellitus, Fever of Unknown Origin, Heart Failure, Hypertension, Pneumonia, Pulmonary Disease, Chronic Obstructive, Urinary Tract Infections, Venous Thrombosis
Enrollment 246 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov