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NCT03436940: PROMENADE
Comparison Between Two Strategies of Discharge Planning for the Reduction of Short Term Hospital Readmissions
NA trial testing On Demand Discharge Planning (DDP) in Patient Discharge in 802 participants. Completed in 13 October 2019.
12 October 2019
Quick facts
| Lead sponsor | A.O.U. Città della Salute e della Scienza |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | crossover |
| Masking | none |
| Primary purpose | other |
| Enrollment | 802 |
| Start date | 1 June 2018 |
| Primary completion | 12 October 2019 |
| Estimated completion | 13 October 2019 |
| Sites | 1 location across Italy |
Drugs / interventions tested
- On Demand Discharge Planning (DDP)
- Routine Discharge Planning (RDP)
Conditions studied
- Patient Discharge — all drugs for Patient Discharge →
Sponsor
A.O.U. Città della Salute e della Scienza — full company profile →
Who can join
18 and older, any sex, with Patient Discharge. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The purpose of this study is to improve discharge planning effectiveness by comparing two strategies \[on-Demand Discharge Planning (DDP) vs. Routine Discharge Planning (RDP)\], in terms of reduction of hospital readmissions for inpatients classified at intermediate risk of complex discharge using the simplified Blaylock Risk Assessment Screening Score (BRASS).
Publications & conference data
1 peer-reviewed publication reference this trial (live from Europe PMC):
-
Routine vs. On-Demand Discharge Planning Strategy in Intermediate-Risk Patients for Complex Discharge: a Cluster-Randomized, Multiple Crossover Trial.
Evangelista A, Camussi E, Corezzi M, Gilardetti M, et al · · 2023 · cited 2× · PMID 37170018 · DOI 10.1007/s11606-023-08186-4
Verify or expand the search:
- PubMed search for NCT03436940
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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Trials by the same sponsor.
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT03436940 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by A.O.U. Città della Salute e della Scienza
- Last refreshed: 29 March 2022
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03436940.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing