Study of Postoperative Chest Tube Management

PHASE4CompletedINTERVENTIONAL
Enrollment

600

Participants

Timeline

Start Date

December 31, 2014

Primary Completion Date

December 18, 2017

Study Completion Date

December 18, 2017

Conditions
Lung Resection
Interventions
OTHER

Reg Pressure

Regulated Suction using the Thopaz+ digital chest drainage device

OTHER

Unreg Pressure

Unregulated Suction using a traditional system (multi-chambered system e.g. Pleur-Evac, Atrium-Maquet or similar device as is routine at each institution)

OTHER

Active Suction (Dig)

Thopaz+ digital chest drainage device set at -20cmH2O at the patient

OTHER

Active Suction (Trad)

Pleur-Evac, Atrium-Maquet or similar set at -20cmH2O at the device.

OTHER

Passive Drainage (Dig)

"Thopaz+ digital chest drainage device set at -8cmH2O at the patient (physiologic)"

OTHER

Passive Drainage (Trad)

"Pleur-Evac, Atrium-Maquet or similar set by gravity (water-seal')"

Trial Locations (5)

18015

St. Luke's Hospital, Bethlehem

30066

WellStar Health System - Kennestone, Marietta

06519

Yale University, New Haven

02215

Beth Israel Deaconess/ Harvard, Boston

07653

Valley Health System, Paramus

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Medela AG

INDUSTRY

lead

Yale University

OTHER