Clinical Trials Sponsored by Regentis Biomaterials

Total 126 results

1
2
3
›

Regentis Biomaterials

Active, not recruiting

Pivotal Study to Evaluate the Safety and Efficacy of GelrinC for Treatment of Cartilage Defects (SAGE)

Articular Cartilage Defects in the Knee Joint

United States
Regentis Biomaterials

Unknown

Study to Evaluate the Safety and Performance of Treatment of Articular Cartilage Lesions Located on the Femoral Condyle With gelrinC

Cartilage Lesion to the Femoral Condyle
Science and biomaterials

Completed

Performance and Safety of the FIXIT® Anchor in Arthroscopic Rotator Cuff Repair (FIXIT®2018)

Rotator Cuff Injuries

France
Silk Biomaterials srl

Unknown

Evaluate the Reconstruction of Digital Nerve Defects in Humans Using an Implanted Silk Nerve Guide

Peripheral Nerve Injury Digital Nerve Hand

Switzerland
Mimetis Biomaterials S.L.

Unknown

The Clinical and Radiographic Outcomes of a 3D-printed Patient-specific Biomimetic Bone Substitute in Maxillofacial Indications: an Interventional, Multi-centred, Open-label, Post-market Clinical Investigation.

Bone Regeneration
Mimetis Biomaterials S.L.

Active, not recruiting

Efficacy of MimetikOss in Alveolar Ridge Preservation Previous to Implant Placement

Alveolar Ridge Preservation

Chile, Spain
PolyNovo Biomaterials Pty Ltd.

Terminated

Randomized Clinical Study Comparing SynPath to Standard of Care in Treatment of Chronic Diabetic Foot Ulcers (DFUs)

Diabetic Foot | Foot Ulcer | Wound Healing | Chronic Foot Ulcer

United States
Turku University Hospital
Bonalive Biomaterials Ltd

Recruiting

Bioactive Glass or Allogenic Bone in Pediatric Bone Cysts

Bone Cysts

Finland
Bonalive Biomaterials Ltd
Turku University Hospital

Active, not recruiting

Clinical Safety and Efficacy of S53P4 Bioactive Glass Putty in Spinal Fusion Surgery

Spinal Deformity | Spine Fusion

Finland
RenJi Hospital
Suzhou SinoMed Biomaterials Co., Ltd

Active, not recruiting

Exploratory Study on Safety of PEEK Knee Prosthesis

Osteoarthritis of the Knee | Rheumatoid Arthritis of Knee

China
Regeneris Medical

Not yet recruiting

Adipose Mesenchymal Cells for Abatement of SARS-CoV-2 Respiratory Compromise in COVID-19 Disease

Covid-19 Pneumonia | Cyotokine Storm
Credentis AG

Completed

Effect of Curodont Repair or Placebo on the Remineralisation in Patients With Class 5 Carious Lesions

Dental Caries

Switzerland
Credentis AG

Completed

Effect of Curodont™ Repair in Patients With Early Approximal Carious Lesions

Dental Caries

Switzerland
Sebastian Findeisen
Bonalive Biomaterials Ltd

Recruiting

Evaluation of the Clinical Effectiveness of Bioactive Glass (S53P4) in the Treatment of Tibia and Femur Non-unions

Pseudoarthrosis of Bone

Germany
Serentis Ltd.

Completed

Phase IIa Safety and Efficacy Study of SRD174 Cream in Patients With AD-associated Pruritus

Pruritus, Atopic Dermatitis

United States
Serentis Ltd.

Completed

Safety and Efficacy of SRD441 Ointment in Patients With Atopic Dermatitis

Atopic Dermatitis

Germany, Bulgaria, Finland
Shenzhen Lando Biomaterials Co., Ltd.
Peking University

Completed

A Clinical Study on the Efficacy and Safety of Lando® Absorbable Collagen Membrane in Oral Bone Repair

Tooth Extraction

China
Credentis AG

Completed

Effect of Curodont Repair in Patients With Early Approximal Carious Lesions

Dental Caries

Switzerland
Regenesis Biomedical, Inc.

Completed

Pilot Study of PEMF Therapy in Treatment of Post-operative Pain Following Total Knee Arthroplasty

Post-Operative Pain Following Total Knee Arthroplasty

United States
Regenesis Biomedical, Inc.

Completed

Study of PEMF (Pulsed Electromagnetic Field) Therapy in the Treatment of Persistent Post-Operative Pain Following Lumbar Surgery

Lumbar Surgery

United States
Regenesis Biomedical, Inc.

Terminated

A Pilot Study of the Provant Therapy System in Subjects With Diabetic Foot Ulcers

Diabetic Foot Ulcers

United States
ASST Ovest Milanese
Hippocrates Research; Bonalive Biomaterials Ltd

Recruiting

RCT on Bioactive Glass S53P4 in Diabetic Foot Osteomyelitis in the Forefoot (DFORCT) (DFORCT)

Osteomyelitis - Foot

Italy
Regenesis Biomedical, Inc.

Completed

Dual Field PEMF Therapy in Lower Extremity Painful Diabetic Distal Symmetric Peripheral Neuropathy (RELIEF)

Diabetic Neuropathy Peripheral

United States
Regenesis Biomedical, Inc.

Completed

A Registry Study to Evaluate Outcomes of PEMF Therapy in Subjects With Various Pain Etiologies

Pain

United States
Regenesis Biomedical, Inc.

Withdrawn

An Open-Label Trial of PEMF Therapy [Provant Infinity Therapy System] for Home Use in Postoperative Pain

Postoperative Pain

United States
Regenesis Biomedical, Inc.

Completed

Study of PEMF to Evaluate VPT and Thermal Sensory in Subjects With Diabetic Peripheral Neuropathy

Diabetic Peripheral Neuropathy

United States
Regenesis Biomedical, Inc.

Terminated

Pulsed Radiofrequency Energy to Treat Post-Bunionectomy Pain

Post-operative Pain

United States
Regenesis Biomedical, Inc.

Completed

A Study to Evaluate PEMF Therapy on Experimentally Inducted Pain in Subjects With Painful Peripheral Diabetic Neuropathy

Painful Peripheral Diabetic Neuropathy

United States
Egetis Therapeutics

Completed

SUNCIST: A Study of Calmangafodipir in Healthy Japanese and Caucasian Subjects

Chemotherapy Induced Peripheral Neuropathy (CIPN)

United States
Egetis Therapeutics

Completed

Mangafodipir as an Adjunct to FOLFOX6 Chemotherapy in Colon Cancer Stage Dukes' C (MANFOL)

Chemotherapy | Colon Cancer

Sweden
Tissue Regenix Ltd

Recruiting

OrthoPureXT Multiligament PMCF Study

Multiligament Knee Injuries

United Kingdom
Tissue Regenix Ltd

Completed

dCell Vascular Patch in Peripheral Vascular Surgery Study for CE Mark Submission

Peripheral Arterial Vascular Occlusion

Hungary, Netherlands
Regenesis Biomedical, Inc.

Completed

Proof of Concept Study of PEMF (Pulsed Electromagnetic Field) Therapy in Subjects With Osteoarthritis of the Knee

Osteoarthritis, Knee

United States
Regenesis Biomedical, Inc.

Completed

Nociceptive Pain Fiber Response

Painful Peripheral Diabetic Neuropathy

United States
Tissue Regenix Ltd

Completed

Clinical Evaluation of dCELL® ACL Scaffold for Reconstruction of the Anterior Cruciate Ligament

Knee Injuries

Poland, Spain, United Kingdom
Joseph M. Still Research Foundation, Inc.
PolyNovo Biomaterials Pty Ltd.

Recruiting

A Randomized, Controlled Trial Comparing the Use of a Biodegradable Temporizing Matrix to Cadaver Skin in the Reconstruction of Hidradenitis Suppurativa Excisions

Hidradenitis Suppurativa

United States
Turku University Hospital
Oulu University Hospital; Turku Clinical Biomaterials Centre

Unknown

Clinical Study of FRC Implant to Treat Skull Bone Defects (Cranio-2)

Cranial Bone Defect | Orbital Base Fracture

Finland
Egetis Therapeutics

Completed

Mangafodipir as an Adjunct to Percutaneous Coronary Intervention (MANAMI)

Myocardial Infarction

Sweden
Tissue Regenix Ltd

Suspended

Clinical Evaluation of dCELL® Meniscus for Partial Replacement of the Meniscus

Knee Injuries

Poland, United Kingdom
Botiss Medical AG
CONVIDIA clinical research GmbH; botiss biomaterials GmbH

Recruiting

Magnesium NOVAMag® Membrane vs. Collagen Jason® Membrane in Patients Requiring Guided Bone Regeneration

Ridge Augmentation | Guided Bone Regeneration (GBR) | Periodontal Bone Defect

Austria, Denmark, Italy
PolyNovo Biomaterials Pty Ltd.
Biomedical Advanced Research and Development Authority

Active, not recruiting

Assessment of Safety and Effectiveness of NovoSorb® BTM in Severe Burns

Burns

United States, India
American Regent, Inc.

Completed

Iron Sucrose In The Treatment of Restless Legs Syndrome: Safety of Three Dose Regimens as Evaluated by Clinical Assessments

Restless Legs Syndrome
American Regent, Inc.

Completed

Efficacy and Safety of Intravenous Ferric Carboxymaltose in Pediatric Patients With Iron Deficiency Anemia and Unsatisfactory Response Oral Iron Under Study Protocol 1VIT17044

Iron Deficiency Anemia

United States
American Regent, Inc.

Completed

Safety and Efficacy of Iron Sucrose in Children

Anemia | Chronic Kidney Disease

United States
American Regent, Inc.

Completed

Efficacy and Safety of Intravenous Ferric Carboxymaltose (FCM) in Patients With Iron Deficiency Anemia (IDA)

Iron Deficiency Anemia

United States
American Regent, Inc.

Completed

Intravenous (IV) Iron vs. No Iron as the Treatment of Anemia in Cancer Patients Undergoing Chemotherapy and Erythropoietin Therapy

Anemia
American Regent, Inc.

Completed

Intravenous (IV) Iron Preparation (VIT-45) in the Treatment of Restless Legs Syndrome (RLS)

Restless Legs Syndrome (RLS)
American Regent, Inc.

Completed

Safety of FCM vs. Standard of Care in Treating Iron Deficiency Anemia in Heavy Uterine Bleeding and Post Partum Patients

Anemia

United States
American Regent, Inc.

Completed

Comparison of the Safety and Efficacy of Intravenous Iron Versus Oral Iron in Subjects Who Display Postpartum Anemia

Anemia

United States
American Regent, Inc.

Withdrawn

Safety Assessment of Iron Sucrose (Venofer) in Patients With Chronic Kidney Disease Who Cannot Tolerate Ferumoxytol (Feraheme) or Iron Dextran (INFed or Dexferrum) (ASSURED)

Iron Deficiency Anemia

United States

1
2
3
›

3

Subscribe