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NCT00341354
Coated Endotracheal Tube and Mucus Shaver to Prevent Hospital-Acquired Infections
Phase 2 trial testing Prolonged Mechanical Ventilation in Infection in 24 participants. Completed in 6 September 2007.
Quick facts
| Lead sponsor | National Heart, Lung, and Blood Institute (NHLBI) |
|---|---|
| Phase | Phase 2 |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Primary purpose | treatment |
| Enrollment | 24 |
| Start date | 27 January 2006 |
| Estimated completion | 6 September 2007 |
| Sites | 1 location across Italy |
Drugs / interventions tested
- Prolonged Mechanical Ventilation
Conditions studied
- Infection — all drugs for Infection →
Sponsor
National Heart, Lung, and Blood Institute (NHLBI)
Who can join
18 and older, any sex, with Infection. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
This study, conducted at the San Gerardo Hospital in Milan, Italy, will examine whether a bacteriocidal-coated endotracheal tube (breathing tube) cleaned with a device called a Mucus Shaver is safe and effective in preventing hospital-acquired infections in patients who require prolonged mechanical ventilation in an intensive care unit (ICU). Pneumonia is the most frequent hospital-acquired infection in the ICU; its development is likely related to the use of a breathing tube. The tube is placed in the patient's trachea (windpipe) to assist breathing during and after an operation. Currently, breathing tubes in intubated patients are cleaned with a suction catheter that draws out secretions that accumulate in the tube. This method does not clean the tube completely, however, and within a few hours after the breathing tube is placed, bacteria may begin to grow inside the tube. Over time, as the patient breathes in and out through the tube, the bacteria may break free and enter the lungs, possibly causing pneumonia. In addition, the growth of bacteria in the tube decreases the size of the airway passage, making it more difficult to keep air moving in and out of the lungs. Previous studies have shown that breathing tubes coated with silver-sulfadiazine prevented bacterial growth in the patient's airways and that use of the Mucus Shaver prevented accumulation of secretions in the lumen of the breathing tube, keeping the tube open. This study will determine if use of the coated tube and Mucus Shaver in patients requiring prolonged mechanical ventilation is safe and if it can reduce bacterial growth, the length of intubation and mechanical ventilation, the occurrence of pneumonia and the length of time in ICU and hospital. Patients at San Gerardo Hospital who are 18 and older, who expect to have a breathing tube in place for more than 48 hours, and who are not allergic to silver-sulfadiazine may be eligible for this study. Participants are randomly assigned to have either a standard breathing tube and standard cleaning or a coated tube cleaned with a Mucus Shaver. At intubation, a sample of secretions is collected from the mouth, the lumen of the breathing tube, and the airways. The lumen of the breathing tube is then cultured every day. When the tube is removed, or on the eighth day of intubation, a sample of secretions is collected from the mouth, the lumen of the breathing tube, and the airways. After the tube is removed, it is examined for biological and microscopic analysis.
Publications & conference data
3 peer-reviewed publications reference this trial (live from Europe PMC):
-
Silver nanoparticles as potential antibacterial agents.
Franci G, Falanga A, Galdiero S, Palomba L, et al · · 2015 · cited 674× · PMID 25993417 · DOI 10.3390/molecules20058856 -
Silver-coated endotracheal tubes for prevention of ventilator-associated pneumonia in critically ill patients.
Tokmaji G, Vermeulen H, Müller MC, Kwakman PH, et al · · 2015 · cited 44× · PMID 26266942 · DOI 10.1002/14651858.cd009201.pub2 -
Nanoparticle-based approaches for bacterial detection and therapy.
Rajana VK, Matireddy A, Miriyals J, Lakshmi KYN, et al · · 2026 · PMID 41748974 · DOI 10.1007/s00253-026-13766-5
Verify or expand the search:
- PubMed search for NCT00341354
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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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 NCT00341354 (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 National Heart, Lung, and Blood Institute (NHLBI)
- Last refreshed: 2 July 2017
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/NCT00341354.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing