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Trial Title:
Intra-operative Air Leak Management After Minimally Invasive Lung Segmental Resection
NCT ID:
NCT06544200
Condition:
Lung Cancer Stage I
Lung; Node
Air Leak From Lung
Conditions: Keywords:
thoracoscopic surgery
Segmentectomy
Air Leak
Hydrogel Matrix
Study type:
Interventional
Study phase:
N/A
Overall status:
Recruiting
Study design:
Allocation:
Randomized
Intervention model:
Parallel Assignment
Primary purpose:
Treatment
Masking:
None (Open Label)
Intervention:
Intervention type:
Device
Intervention name:
Polymeric Hydrogel Matrix
Description:
application of Polymeric Hydrogel Matrix along the suture line at the completion of lung
resection
Arm group label:
Polymeric Hydrogel Matrix
Summary:
In patients undergoing minimally invasive thoracoscopic surgery (video-assisted
thoracoscopic surgery, or VATS), a still unsolved issue is represented by intraoperative
alveolar air leaks (IOAALs), which if prolonged beyond the fifth postoperative day can
lead to higher risk of complications and higher medical costs. The polymeric hydrogel
matrix (PHM) is a novel tool to manage intraoperative IOAALs. The primary end-point of
our study was to verify whether PHM would be able to reduce postoperative air leaks;
secondary end-points were the possible reduction of the permanence time of the chest
drain (CD) and the hospital length (HL) in the PHM group compared with no treatment.
Detailed description:
The management of postoperative air leaks remains an unresolved issue in pulmonary
resections. This complication can be present in up to 75% of patients undergoing major
lung resections; however, it often resolves spontaneously. In 8% of cases, air leaks can
persist for up to 5-7 days post-surgery, and are associated with a higher risk of
complications, such as prolonged chest tube duration, increased incidence of
postoperative infections and higher medical and non-medical costs. Sealants are
non-invasive medical devices that help reduce or eliminate air leaks and bleeding. A
recent study showed an increased risk of air leaks in patients undergoing segmentectomies
compared to lobar resections; this study is designed to evaluate the efficacy of
intraoperative use of Polymeric Hydrogel matrix in achieving aerostasis during anatomical
segmental pulmonary resections via VATS or RATS, compared to patients receiving standard
of care. All patients meet the eligibility criteria and successfully undergo a minimally
invasive segmentectomy will undergo intraoperative evaluation of alveolar air leaks.
Those with moderate air leaks (30-60 ml/respiratory act, measured at the Ventilation
Mechanical Test, which consists in 1 minute volumetric ventilation with a constant flow
and a peak pressure of 22 cmH2O, 12 respiratory rates per minute and a positive
end-expiratory pressure (PEEP) of 5 cmH2O), will be randomized to receive Polymeric
Hydrogel matrix or no further treatment.The primary endpoint is to evaluate the efficacy
in reducing postoperative air leaks secondary to the intraoperative application of
Polymeric Hydrogel matrix (measured in days from the first postoperative day to the last
day the air leaks are detected), compared to a control group receiving standard of
care.The secondary endpoints include the evaluation of the postoperative permanence of
chest tube, total length of hospital stay, medical and non-medical costs and
postoperative complications up to 40 days of follow-up.
Criteria for eligibility:
Criteria:
Inclusion Criteria:
- patients aged > 18 years
- undergoing anatomical pulmonary resection (segmentectomy) via VATS or RATS
- benign and/or malignant lung disease
- No known allergy to any of the components of the device
Exclusion Criteria:
- Refusal or inability to give informed consent to the study protocol
- Age < 18 years
- Pregnancy
- Chronic Kidney Failure
- Allergies or contraindications to any of the Polymeric Hydrogel Matrix components
- Patients undergoing pulmonary resections different than segmentectomy (wedge,
lobectomy, bilobectomy, pneumonectomy)
- Patients undergoing open surgery
- More than one chest tube after lung resection
Gender:
All
Minimum age:
18 Years
Maximum age:
N/A
Healthy volunteers:
No
Locations:
Facility:
Name:
Thoracic Surgery Unit
Address:
City:
Padua
Zip:
35128
Country:
Italy
Status:
Recruiting
Contact:
Last name:
MARCO MAMMANA, MD,PhD
Phone:
+390498212442
Email:
marco.mammana@aopd.veneto.it
Start date:
July 15, 2023
Completion date:
July 1, 2025
Lead sponsor:
Agency:
University Hospital Padova
Agency class:
Other
Source:
University Hospital Padova
Record processing date:
ClinicalTrials.gov processed this data on November 12, 2024
Source: ClinicalTrials.gov page:
https://clinicaltrials.gov/ct2/show/NCT06544200