43 studies found for:    INFUSE | Industry
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Rank Status Study
1 Completed
Has Results
Study of Techniques of Subcutaneous Administration of Fluids Enabled by Human Recombinant Hyaluronidase
Condition: Dehydration
Intervention: Drug: hylenex-facilitated subcutaneous Lactated Ringer's infusion
2 Completed
Has Results
Study of Subcutaneous Hydration Enabled by Human Recombinant Hyaluronidase (Hylenex)
Condition: Healthy
Intervention: Drug: recombinant human hyaluronidase
3 Terminated
Has Results
Study of In-line Pressure Using Various Techniques of Subcutaneous Administration of Fluids Enabled by Human Recombinant Hyaluronidase (INFUSE-AT1A)
Condition: Dehydration
Intervention: Drug: Subcutaneous HYLENEX (recombinant human hyaluronidase) and Lactated Ringer's solution
4 Withdrawn Clinical Study of INFUSE® Bone Graft Compared to Autogenous Bone Graft for Vertical Ridge Augmentation
Conditions: Alveolar Bone Loss in Mandible;   Edentulous Alveolar Ridge In Mandible
Interventions: Device: INFUSE® Bone Graft;   Procedure: Autogenous bone graft from tibia or iliac crest
5 Completed
Has Results
Study of Subcutaneous Rehydration With Recombinant Human Hyaluronidase for Infants and Children
Condition: Dehydration
Intervention: Drug: hyaluronidase (human recombinant)/rehydration fluid
6 Completed
Has Results
Pharmacokinetic and Safety Study of HYLENEX Recombinant-Augmented Subcutaneous Ceftriaxone Administration
Condition: Healthy
Interventions: Drug: SC HYLENEX and Ceftriaxone;   Drug: SC Placebo and Ceftriaxone;   Drug: IV Ceftriaxone
7 Terminated Sinus Augmentation With Dental Implant
Condition: Maxillary Sinus Bone Loss
Intervention: Device: INFUSE® Bone Graft
8 Terminated Localized Alveolar Ridge Augmentation With Space Maintenance Devices
Condition: Alveolar Bone Loss
Intervention: Device: INFUSE® Bone Graft
9 Terminated Localized Alveolar Ridge Augmentation With Dental Implant
Condition: Alveolar Bone Loss
Intervention: Device: INFUSE® Bone Graft
10 Withdrawn Efficacy and Time and Resources for Hylenex-facilitated SC Rehydration Versus ORT for Dehydrated Children in the Emergency Department (ED)
Condition: Dehydration
Interventions: Other: Oral rehydration fluid;   Drug: Isotonic hydration fluid and recombinant human hyaluronidase
11 Completed INFUSE Morphine Study
Condition: Pain
Intervention: Drug: Hylenex
12 Suspended INFUSE®Bone Graft in Transforaminal Lumbar Interbody Fusion for Degenerative Disease of Lumbosacral Spine
Condition: Lumbar Spine Degeneration
Interventions: Device: INFUSE Bone Graft;   Other: Iliac Crest Bone Graft
13 Completed
Has Results
INFUSE® Bone Graft/ PEEK Interbody Spacer/ Anterior Cervical Plate Pivotal Clinical Trial
Condition: Degenerative Disc Disease
Intervention: Device: INFUSE® Bone Graft/PEEK Spacer/Anterior Cervical Plate
14 Completed Actifuse ABX Versus INFUSE in Posterolateral Instrumented Lumbar Fusion
Condition: Degenerative Disc Disease
Interventions: Procedure: Actifuse ABX;   Procedure: INFUSE, plus Mastergraft granules
15 Completed Actifuse ABX Versus INFUSE in Posterolateral Instrumented Lumbar Fusion (PLIF) With Interbody Fusion
Condition: Degenerative Disc Disease
Interventions: Procedure: Actifuse ABX;   Procedure: INFUSE, plus master granules (MGG)
16 Terminated Tibial Delayed Healing Pivotal Clinical Trial
Condition: Tibial Delayed Healing
Interventions: Device: Open implantation of INFUSE Bone Graft (rh BMP-2);   Procedure: Open implantation of ICBG
17 Completed INFUSE® Bone Graft and MASTERGRAFT® Granules With CD HORIZON® for Posterolateral Lumbar Fusion in Patients With Degenerative Disc Disease - Pilot Study
Condition: Degenerative Disc Disease
Interventions: Device: INFUSE® Bone Graft/MASTERGRAFT® Granules/CD HORIZON®;   Device: Autogenous Bone / CD HORIZON® Spinal System
18 Completed TELAMON P™ Implant/INFUSE® Bone Graft/CD HORIZON® Spinal System Pilot Study
Condition: Degenerative Disc Disease
Intervention: Device: TELAMON P™ /INFUSE® Bone Graft/CD HORIZON® Spinal System
19 Completed INFUSE™ BONE GRAFT/CORNERSTONE-SR™ Allograft Ring/ATLANTIS™ Anterior Cervical Plate- Pilot Study
Condition: Degenerative Cervical Disc Disease
Interventions: Device: INFUSE™ Bone Graft/CORNERSTONE-SR™ /ATLANTIS™;   Device: Autogenous bone/CORNERSTONE-SR™ /ATLANTIS™
20 Terminated INFUSE ® Bone Graft/CORNERSTONE-SR® Allograft Ring/ATLANTIS® Anterior Cervical Plate System Pivotal Trial
Condition: Degenerative Cervical Disc Disease
Interventions: Device: INFUSE™ Bone Graft/CORNERSTONE-SR™ /ATLANTIS™;   Device: Autogenous bone/CORNERSTONE-SR™ /ATLANTIS™

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Indicates status has not been verified in more than two years