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NCT04511091: VATS
Studio Osservazionale Retrospettivo Uneventful Vatslobectomy: Caratteristiche Cliniche All'Interno Del Registro Vats Group
trial testing VATS lobectomy in Thoracic Surgery, Video-Assisted in 10,000 participants. Completed in 1 July 2020.
1 May 2020
Quick facts
| Lead sponsor | University Hospital of Ferrara |
|---|---|
| Status | Completed |
| Study type | OBSERVATIONAL |
| Enrollment | 10,000 |
| Start date | 1 January 2014 |
| Primary completion | 1 May 2020 |
| Estimated completion | 1 July 2020 |
Drugs / interventions tested
- VATS lobectomy
Conditions studied
- Thoracic Surgery, Video-Assisted — all drugs for Thoracic Surgery, Video-Assisted →
Sponsor
University Hospital of Ferrara
Who can join
Eligibility, any sex, with Thoracic Surgery, Video-Assisted. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
Background VATS lobectomy centers face pressure to reduce hospitalization to contain costs, and some centers have sought to develop "fast-track" protocols. There are limited data to identify which patients would be appropriate for fast-tracking. Objective The first objective was to identify factors associated to short lenght of stay after VATS lobectomy. The second objective was to verify the influence of these variables in uncomplicated VATS lobectomy. Methods We reviewed all thoracoscopic lobectomies for cancer operations reported to the Italian VATS Group between January 2014 and January 2020. Patient and procedural characteristics, length of stay and 30-day morbidity and mortality were reviewed. Patients were divided into two subgroups depending on their reaching the targeted length of stay (≤ or \> 4 days). The association between preoperative and intraoperative variables and postoperative length of stay (LOS) ≤ 4 days was assessed using a stepwise multivariate logistic regression analysis to identify factors independently associated with LOS and factors related to LOS in uncomplicated cases.
Publications & conference data
No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.
Verify or expand the search:
- PubMed search for NCT04511091
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Related trials
Other trials of VATS lobectomy
Trials testing the same drug.
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- NCT04799509 — Assessment of the 90-day Mortality Risk Score After VATS Lobectomy · completed
Other University Hospital of Ferrara trials
Trials by the same sponsor.
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- NCT06679517 — Observational Study Relating to the Long-term Follow-up of Patients with Severe Aortic Stenosis Evaluated for Percutaneo · enrolling by invitation
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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 NCT04511091 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by University Hospital of Ferrara
- Last refreshed: 12 August 2020
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/NCT04511091.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing