TORQ Clinical Study — TORQClin

Post Cardiac Surgery Clinical Trial

Official title:
The Influence of the TORQ Sternal Closure Assistance Device on Post-Operative Pain, Pulmonary Function and Quality of Life Compared to Traditional Manual Wire Closure: A Randomized Controlled Trial.

Status Completed

Clinical Trial Summary

The proposed trial is to evaluate the use of the TORQ closure assistance device and how it affects pain in the sternum, breathing and quality of life compared to traditional use of needle drivers or similar to close sternal wires.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Intervention Model: Single Group Assignment, Masking: Double Blind (Subject, Caregiver), Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT01647178
Study type	Interventional
Source	Kardium Inc.
Contact
Status	Completed
Phase	N/A
Start date	March 2012
Completion date	October 2013

View Details

See also
Status	Clinical Trial	Phase
Withdrawn	`NCT01463345` - Blood Conservation in Cardiac Surgery	N/A
Completed	`NCT02829203` - Pre-Frailty Risk in Cardiovascular Surgery	N/A
Completed	`NCT01941667` - Transitional Telehealth Home Care: REACH	N/A
Completed	`NCT02569008` - Minimal Volume for Fluid Challenge in Post-operative Patients	N/A
Recruiting	`NCT02146196` - Robotic Assisted Rehabilitation for Heart Failure Patients and Patients After Cardiac Surgery	N/A
Completed	`NCT01662141` - Measure Cardiac Output Using Ultrasound Dilution in Mechanically Ventilated Children	N/A
Completed	`NCT02659982` - Evaluation of EarlySense Home Care Tele-monitoring Device -For Early Detection of Deterioration For Cardiac Patients at Home	N/A