Clinical trials: Spinal Fusion Acquired
Spinal Fusion Acquired, Fusion of Spine (Disease)
Efficacy and Safety of SurgiFill™ on Spinal Fusion
This study was designed to investigate the safety and efficacy of SurgiFill™, a bone grafting material, in patients with spinal fusion.
- Trial name
- NCT02466048
- Testing
- Spinal Fusion, SurgiFill™
- Where
- 2 sites in South Korea
- Volunteers
- 20 people, healthy volunteers welcome
- Sponsor
- Cellontech Co., Ltd.
Spinal Fusion Acquired
Intrawound Vancomycin Powder in Spinal Fusion Surgery
Vancomycin powder (for solution for Infusion) will be investigated (off-label usage) in spinal fusion surgery. The powder will be locally administered into to the wound cavity before wound closure.
- Trial name
- iVRCT (NCT02631408)
- Testing
- Vancomycin
- Where
- Austria
- Volunteers
- 308 people
- Sponsor
- Orthopedic Hospital Vienna Speising
Spinal Fusion Acquired, Spinal Stenosis
Intraoperative Infusion of Precedex to Reduce Length of Stay After Lumbar Spine Fusion
Major lumbar spine surgery causes inflammation, soreness and swelling that can delay discharge from the hospital. Dexmedetomidine (DEX) has been shown to have anti-inflammatory effects.
- Conditions
- Spinal Fusion Acquired, Spinal Stenosis, Lesions of Lumbosacral Intervertebral Disc, Spinal Diseases
- Trial name
- DEXREDLOS (NCT00808665)
- Testing
- Dexmedetomidine, 0.9% Saline
- Where
- United States
- Volunteers
- 68 people
- Sponsor
- Vanderbilt University Medical Center
Acquired Bleeding Disorder, Spinal Fusion
Use of Activated Recombinant FVII in Spinal Surgery
This trial is conducted in the United States of America (USA). The purpose of this clinical research trial is to understand how safe and effective Recombinant Activated FVII is for reducing bleeding and blood transfusions in…
- Trial name
- NCT00102037
- Testing
- eptacog alfa (activated)
- Where
- 14 sites in United States
- Volunteers
- 50 people
- Sponsor
- Novo Nordisk A/S
Degenerative Spinal Disease, Elderly Patients
Preoperative Risk Evaluation and Per ERAS Intervention in the Chinese Elderly Patients Underwent Spinal Fusion Surgery
This study aims to evaluate the value of preoperative risk factor evaulation combined with perioperative ERAS measures in improving the clinical prognosis of elderly patients undergo the spinal fusion.
- Conditions
- Degenerative Spinal Disease, Elderly Patients, Spinal Fusion Acquired
- Trial name
- NCT06607081
- Testing
- Multidisciplinary Preoperative Risk Evaluation and the Corresponded Pre ERAS intervention
- Where
- 2 sites in China
- Volunteers
- 5,000 people
- Sponsor
- Xijing Hospital