Clinical Trials Logo

Clinical Trial Summary

The investigators will define the most appropriate safe dose of D50 to heal air leaks in patients that have undergone lung resection surgery


Clinical Trial Description

The investigators will define the most appropriate safe dose of D50 to heal air leaks in patients that have undergone lung resection surgery (Phase I study). Air leaks from unhealed lung tissue are one of the most common complications after lung surgery including wedge resection, segmentectomy and lobectomy. Air leaks can lead to a delay in chest tube removal, prolonged pain, increased infections, prolonged hospital stay, and increased costs to the health care system. Different agents have been used to heal air leaks by creating a pleurodesis (adhesions to obliterate the pleural space between the visceral and parietal pleura). The success with these agents has been variable and come with the cost of complications that have restricted their use the post-operative period. There has been recent interest in the use of 50% hypertonic glucose (D50) to create pleurodesis with encouraging reports coming mostly from Asia. The investigators have performed a pilot study using 180 mL of D50 instilled through the chest tube for the management of post lobectomy air leak with very encouraging results. This preliminary study used strict inclusion criteria of only lobectomy patients and excluded all patients with known diabetes or any postoperative hyperglycemia. It is unknown if these patients would have benefitted from D50. Also, the optimal dose of D50 was chosen empirically and never clearly defined by previous work. It has been reported that high doses of D50 have been associated with acute lung injury. It is therefore critical that the optimal safe dose is clarified. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03905408
Study type Interventional
Source Lawson Health Research Institute
Contact
Status Completed
Phase Phase 1
Start date September 17, 2019
Completion date February 1, 2021

See also
  Status Clinical Trial Phase
Recruiting NCT05628415 - Comparison Between the Non-powered AEON™ Endostapler and Echelon FLEX™ Powered Plus Stapler With Regards to the Closure of Lung Tissue After Lung Resection in the Presence of Severe Lung Emphysema N/A
Recruiting NCT02502643 - The Efficacy of OK-432 Pleurodesis on Postoperative Air Leak N/A
Recruiting NCT05638113 - Prolonged Air Leakage After Major Lung Resection N/A
Completed NCT04065880 - Neoveil® Versus TachoSil® for the Treatment of Pulmonary Air Leaks Following Lung Operation N/A