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Comparison of 16F Versus 24F Chest Drain After Minimally Invasive Pulmonary Lobectomy and/or Segmentectomy: a Monocentre Prospective Randomized Controlled Trial

Status: Recruiting
Location: See location...
Intervention Type: Procedure, Device
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The aim of the study is to evaluate postoperative pain in patients receiving a small-bore (16F) chest drain compared to those receiving the standard large-bore (24F) chest drain after minimally invasive pulmonary lobectomy and/or segmentectomy.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Informed Consent signed by the patient (all sex and gender)

• Patients' age from ≥ 18 to no age limit at time of study inclusion

• American Society of Anaesthesiologists (ASA) physical status classification I to IV

• Patients with resectable non-small cell lung cancer (NSCLC) deemed operable by minimally invasive surgical technique.

• Minimally invasive anatomical lung resections under general anaesthesia: lobectomy, lobectomy with wedge resection, lobectomy combined with segmentectomy, segmentectomy with wedge resection, bilobectomy

Locations
Other Locations
Switzerland
University Hospital Basel
RECRUITING
Basel
Contact Information
Primary
Helga Bachmann, MSc Clinical Research
helga.bachmann@usb.ch
+41 (0)61 328 71 70
Backup
Makhmudbek Mallaev, MD
makhmudbek.mallaev@usb.ch
+41 (0)61 556 51 89
Time Frame
Start Date: 2025-05-01
Estimated Completion Date: 2027-08-30
Participants
Target number of participants: 124
Treatments
Experimental: 16F - early removal
small-bore (16F) chest tubes, removal 2h until 6h after end of skin closure
Experimental: 16F - standard removal
small-bore (16F) chest tubes, removal 1 day postoperative
Experimental: 24F - early removal
large-bore (24F) chest tubes, removal 2h until 6h after end of skin closure
Active_comparator: 24F - standard removal
large-bore (24F) chest tubes, removal 1 day postoperative
Related Therapeutic Areas
Sponsors
Leads: University Hospital, Basel, Switzerland

This content was sourced from clinicaltrials.gov