Clinical Trials Sponsored by Firstkind Ltd

Total 17070 results

Firstkind Ltd

Active, not recruiting

Geko™ Cross Therapy Registry - Wound (CTR-Wound)

Diabetic Foot Ulcer | Venous Leg Ulcer | Wound | Arterial Leg Ulcer

United Kingdom, United States
Firstkind Ltd

Completed

Efficacy Study for Geko Device in VLU Patients

Leg Ulcer | Venous Leg Ulcer | Wound | Wound Leg | Leg Ulcers Venous

United Kingdom
Firstkind Ltd

Terminated

Speckle Study: In Arterial, Mixed and Diabetic Foot Ulcers

Leg Ulcer

United Kingdom
Firstkind Ltd

Completed

Geko Neuromuscular Stimulator vs Thromboembolism Deterrent Stockings (TEDS): DVT Prevention Study

Deep Vein Thrombosis

United Kingdom
Firstkind Ltd

Completed

Study of gekoTM Interaction With Cardiac Pacemakers

Stroke | Wound Heal | Cardiac Pacemaker Electrical Interference | Edema Leg

United Kingdom
Firstkind Ltd

Completed

Optimization of Onpulse Technology for Patients With Post Surgical or Vascular Oedema (TURBO)

Neuropathy | Oedema

United Kingdom
Firstkind Ltd

Terminated

Efficacy Study for Geko Device in VLU Patients (Canada)

Leg Ulcer | Venous Leg Ulcer | Venous Ulcer

Canada
Firstkind Ltd

Completed

Cross Therapy Registry - Edema - US (CTR-Edema-US)

Edema Leg

United States
Firstkind Ltd

Completed

A Study in Patients With Venous Leg Ulcers and Measuring the Effects of Using Geko™ Device

Venous Leg Ulcer

United Kingdom
Firstkind Ltd

Completed

Geko Venous Leg Ulcer Study

Venous Leg Ulcer

United Kingdom
Firstkind Ltd

Withdrawn

Intermittent Pneumatic Compression of the Foot vs Geko Plus R-2 Neuromuscular Electrostimulation Device in Venous Leg Ulcer Patients

Venous Leg Ulcer
Firstkind Ltd

Completed

Firefly ANKLE Sprain Study

Grade I/II Ankle Sprain

United Kingdom
Firstkind Ltd

Not yet recruiting

Geko™ KM40C Hydrogel Skin Adhesion Trial (XW-3)

Leg Ulcer

United Kingdom
Firstkind Ltd

Recruiting

Foot and Ankle Post-operative Oedema Management Using Geko™

Edema | Surgery

Spain, United States, United Kingdom
Firstkind Ltd

Completed

Efficacy of Adhesive Strength of New Hydrogel Formulation

Stroke, Acute

United Kingdom
Firstkind Ltd

Suspended

Cross Therapy Registry - Oedema - EU (CTR-Oedema-EU) (CTR-Oedema-EU)

Edema Leg

Belgium
Firstkind Ltd

Completed

Feasibility Study of the Use of the gekoTM Device for Faecal Incontinence in Older People Living at Home or in Care Homes

Fecal Incontinence

United Kingdom
Firstkind Ltd

Withdrawn

IPC-CALF Versus GEKO in Post-op Total Hip Patients

Total Hip Replacement
Firstkind Ltd

Completed

Midds Ankle Fracture

Ankle Fracture Requiring Internal Fixation

United Kingdom
Firstkind Ltd
Loughborough University

Completed

Neuromuscular Electrical Stimulation Via the Peroneal Nerve Reduces Muscle Soreness Following Intermittent Exercise

Delayed Onset Muscle Soreness

United Kingdom
moveUP bv
Firstkind Ltd

Recruiting

The Post-operative Effect on Formation of Oedema After Total Knee Arthroplasty With or Without the Use of a Nerve Stimulator (the gekoTM Device)

Joint Diseases | Osteoarthritis, Knee | Rehabilitation | Edema Leg

Belgium
Hampshire Hospitals NHS Foundation Trust
Firstkind Ltd

Completed

Lower Limb Blood Flow Geko vs Foot Pump

Venous Thrombosis | Arthroplasty, Replacement, Hip
University of Manchester
Manchester University NHS Foundation Trust; Firstkind Ltd

Unknown

Wound Healing Process in Diabetic Neuropathy and Diabetic Neuroischemia (Geko)

Diabetes
Manchester University NHS Foundation Trust
Manchester Academic Health Science Centre; Firstkind Ltd

Recruiting

Neuromuscular Stimulation Versus Intermittent Compression for Venous Thromboembolism Prophylaxis in Critical Care (ENSARIA)

Sepsis | Critical Illness | Venous Thromboembolism | Acute Illness

United Kingdom
Firstkind Ltd
National Institute for Health Research, United Kingdom; University of California and other collaborators

Recruiting

GEKO Venous Thromboembolism Prevention Study

Deep Vein Thrombosis | Venous Thromboembolism | Stroke, Acute | Pulmonary Embolism

United Kingdom
University of Washington
National Institute of General Medical Sciences (NIGMS); Firsthand Technology...

Completed

Firsthand ID for Pain Control (ID)

Virtual Reality Pain Distraction

United States
Mirka Ltd
Clinius Ltd

Completed

A Pre-market Study to Evaluate the Performance and Safety of a Skin Preparation Device for Removal of Dry Crusty Skin

Keratosis, Actinic | Hyperkeratotic Callus | Actinic Lesion | Solar Keratosis/Sunburn | Hyperkeratosis | Hyperkeratotic; Lesion | Hyperkeratotic Actinic Keratosis

Finland
Salus Ltd.
TheraVitae Ltd.

Completed

Autologous Angiogenic Cell Precursors (ACPs) for the Treatment of Peripheral Artery Disease

Critical Limb Ischemia

Hungary
Janssen-Cilag Farmaceutica Ltda.
Janssen Korea, Ltd., Korea

No longer available

An Expanded Access Program for Decitabine in Patients With Myelodysplastic Syndrome (MDS)

Myelodysplastic Syndromes

Hong Kong, Brazil, Thailand
Paion UK Ltd.
Chiltern International Ltd.; HFL Ltd.

Completed

An Efficacy and Safety Study to Compare Morphine 6-glucuronide (M6G) and Morphine in Patients Suffering With Post-Operative Pain for at Least 24 Hours

Postoperative Pain

France, Germany, Netherlands, Poland, United Kingdom, Czechia
Calcivis Ltd
Medsource UK Ltd.

Completed

Caries Lesion Activity in Orthodontic Patients - Calcivis System

Dental Caries

United Kingdom
Cardiovalve Ltd.
Meditrial Europe Ltd.

Recruiting

Cardiovalve Transfemoral System - FIM Study

Mitral Regurgitation

Lithuania
Vensica Therapeutics Ltd.
Blueclinical, Ltd.

Completed

Clinical Trial for the Assessment of Safety, Usability and Efficacy of the Vixe Combination for OAB in Female Subjects (XAVIER)

Overactive Bladder

Portugal
Nanomedic Technologies Ltd.

Completed

Evaluation of the SpinCare™ System in the Treatment of Partial Thickness Burns (SPINCARE2)

Partial Thickness Burn

Israel
Nanomedic Technologies Ltd.

Completed

Evaluation of the SPINNER Device for the Application of Wound Dressing: Treatment of Split Skin Graft Donor Sites (SPINNER01)

Wound of Skin

Israel
Danisco
4Pharma Ltd.; Medfiles Ltd.

Completed

Next Generation Probiotics (NGPs) for Metabolic Health

Microbial Colonization
Calcivis Ltd
Medsource UK Ltd.

Completed

Safety and Performance Evaluation of the Calcivis System

Dental Caries

United Kingdom
Targia Pharmaceuticals Ltd.
SoluBest Ltd.

Unknown

Comparative Bioavailability Study of Omexa Sumatriptan vs. Imitrex® in Healthy Volunteers

Migraine
Xention Ltd
Ario Pharma Ltd

Completed

A Study to Assess the Efficacy of XEN-D0501 in Reducing the Cough Frequency in Patients With COPD

Chronic Obstructive Pulmonary Disease

United Kingdom
TyrNovo Ltd.

Active, not recruiting

A Study to Evaluate NT219 Alone and in Combination With ERBITUX® (Cetuximab) in Adults With Advanced Solid Tumors and Head and Neck Cancer

Head and Neck Cancer | Squamous Cell Carcinoma of Head and Neck | Metastatic Solid Tumor | Colorectal Adenocarcinoma | Solid Tumor, Adult | Recurrent Solid Tumor

United States, Israel
Xention Ltd
Ario Pharma Ltd

Completed

A Study to Assess the Efficacy of XEN-D0501 in Reducing the Cough Frequency in Patients With Chronic Idiopathic Cough

Chronic Idiopathic Cough

United Kingdom, Ireland
Neurovalens Ltd.
University College Dublin; Exploristics Ltd; Compliance Solutions Ltd.

Completed

Effect of VeSTAL Device in Type 2 Diabetes Mellitus

Metabolic Syndrome | Type 2 Diabetes

Ireland
Neurovalens Ltd.
University College Dublin; Exploristics Ltd; Compliance Solutions Ltd.

Completed

Electrical Vestibular Nerve Stimulation (VeNS) Compared to Sham Control as a Means of Reducing Excess Body Weight

Obesity | Overweight | Metabolic Syndrome | Overweight and Obesity | Overweight or Obesity

Ireland
Nemysis Ltd
RDC Clinical Pty Ltd

Recruiting

Safety and Effectiveness of Iron Hydroxide Adipate Tartrate (IHAT) in Iron Deficient Premenopausal Women

Iron-deficiency

Australia
Nuritas Ltd
RDC Clinical Pty Ltd

Recruiting

Effects of PeptiSleep in Healthy Males and Females With Mild to Moderate Sleep Impairment

Sleep

Australia
Respirent Pharmaceuticals Co Ltd.
Becro Ltd.

Recruiting

Bioequivalence With Clinical Endpoint Study of Fluticasone Propionate 100 mcg and Salmeterol 50 mcg Inhalation Powder/Respirent Pharmaceuticals vs. ADVAIR DISKUS® 100/50 mcg Inhalation Powder/GSK in Patients With Asthma (AERO-PD)

Asthma

Greece
Akaza Bioscience Ltd
Iqvia Pty Ltd

Not yet recruiting

TAK-242 in Patients With Acute Alcoholic Hepatitis

Acute-On-Chronic Liver Failure
Persica Pharmaceuticals Ltd
Micron Research Ltd

Active, not recruiting

Persica 002 Phase 1b PP353 vs Placebo in the Treatment of Low Back Pain

Chronic Low-back Pain

Spain, United Kingdom, New Zealand, Denmark
Respirent Pharmaceuticals Co Ltd.
Becro Ltd.

Completed

A Clinical Trial for Examining the Therapeutic Equivalence Between Fluticasone Propionate 100 mcg/Blister Oral Inhalation Powder/Respirent Pharmaceuticals vs. FLOVENT DISKUS® 100mcg/Blister Oral Inhalation Powder/GSK in Patients With Asthma (ANASSA-PD)

Asthma

Greece
Respirent Pharmaceuticals Co Ltd.
Becro Ltd.

Active, not recruiting

A Bioequivalence Study Between Fluticasone Propionate 250 mcg and Salmeterol Xinafoate 50 mcg Inhalation Powder/Respirent Pharmaceuticals vs. ADVAIR DISKUS® 250/50 Inhalation Powder/GSK in Healthy Volunteers

Asthma | Bioequivalence

Greece

Clinical Trials Sponsored by Firstkind Ltd

Sponsors and Collaborators

Medical Conditions

Drug Interventions

CROs by country

CROs in Netherlands

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Drug Interventions

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