| Not Yet Recruiting | Clinical Efficacy of Stopping Oral Antibiotics When Symptoms Stop, Compared to 'Finishing the Course' NCT07532941 | Murdoch Childrens Research Institute | Phase 4 |
| Not Yet Recruiting | Validation of the Use of the Arteriovenous Tension Difference in CO2 Under Hyperbaric Conditions NCT07492030 | University Hospital, Lille | — |
| Recruiting | Perspectives on Antibiotics and Tracking Symptoms in Children NCT07093749 | Murdoch Childrens Research Institute | N/A |
| Recruiting | Intravenous Versus Oral Treatment of the Main Acute Infections NCT06715306 | University of Southern Denmark | N/A |
| Active Not Recruiting | Quasi-Randomized Evaluation of the UCLA Next Day Clinic (NDC) NCT06526884 | University of California, Los Angeles | N/A |
| Enrolling By Invitation | High-dose Cephalexin for Cellulitis (HI-DOCC) NCT05852262 | Ottawa Hospital Research Institute | Phase 4 |
| Unknown | Benchtop NMR Spectroscopy for Assessment of Clinical Human Pathologies (BRANCH-P STUDY) NCT05473325 | Willows Health | — |
| Completed | Decreasing Antibiotic Duration for Skin and Soft Tissue Infection Using Behavioral Economics in Primary Care NCT05226260 | Nationwide Children's Hospital | N/A |
| Completed | High-dose vs. Standard-dose Cephalexin for Cellulitis NCT04471246 | Ottawa Hospital Research Institute | Phase 4 |
| Completed | Utility of Thermal Imaging in Diagnosis of Cellulitis for Lower Extremity Complaints in the Emergency Departme NCT04928235 | University of Wisconsin, Madison | — |
| Completed | The Personalised Antibiotic Duration for Cellulitis (PAD-C) Study NCT05023200 | University of Sussex | — |
| Completed | Continuous Temperature Telemonitoring of Patients With COVID-19 and Other Infectious Diseases in Hospital at H NCT05959928 | Vitio Medical S.L. | — |
| Completed | RECELL® System Combined With Meshed Autograft for Reduction of Donor Skin Harvesting in Soft Tissue Reconstruc NCT04091672 | Avita Medical | N/A |
| Completed | Radiofrequency and Targeted Pressure Energy for Cellulite Reduction NCT05624216 | BTL Industries Ltd. | N/A |
| Completed | Improving Safety of Diagnosis and Therapy in the Inpatient Setting NCT04393909 | Brigham and Women's Hospital | N/A |
| Unknown | Prevention of Vaginal Cellulitis or Vaginal Cuff Abscess After Laparoscopic Hysterectomy NCT03917134 | CES University | N/A |
| Unknown | A Subjective Observational Study of Patients Using Medicated Footbath/Footwash Treatment in Podiatry Care NCT03781024 | Data Collection Analysis Business Management | — |
| Completed | Handheld Infrared Thermometer to Evaluate Cellulitis NCT03846635 | McGill University Health Centre/Research Institute of the McGill University Health Centre | — |
| Terminated | Point-of-Care Ultrasound Educational Initiative for Insect Bites NCT03619746 | New York City Health and Hospitals Corporation | N/A |
| Completed | The Effects of Iontophoresis in Women With Gynoid Hidrolipodystrophy. NCT03556917 | Universidade Norte do Paraná | Phase 2 / Phase 3 |
| Completed | The Effect of Histopathologic Analysis and Tissue Cultures on Inpatient Management of Cellulitis and Pseudocel NCT03785834 | Ohio State University | — |
| Completed | Effectiveness of Diathermy-Radiofrecuency Compared With Cavitation in Cellulitis Treatment NCT03474523 | University of Cadiz | N/A |
| Unknown | Effect of Vibro-oscillatory Therapy for Improvement of Body Contour and Appearance of Cellulite. NCT03312946 | Indústria Brasileira Equipamentos Médicos - IBRAMED | N/A |
| Completed | Shock Waves for Treatment of Gynoid Lipodystrophy and Localized Fat NCT03275259 | Indústria Brasileira Equipamentos Médicos - IBRAMED | N/A |
| Unknown | Penicillin for the Emergency Department Outpatient Treatment of CELLulitis NCT02922686 | Royal College of Surgeons, Ireland | Phase 4 |
| Completed | Evaluation of Implementation of a National Point-of-Care Ultrasound Training Program NCT03296280 | VA Office of Research and Development | — |
| Completed | Hospitalization at Home: The Acute Care Home Hospital Program for Adults NCT02864420 | Brigham and Women's Hospital | N/A |
| Completed | The Effect of Dermatology and Teledermatology Consultations on Length of Hospital Admission, 30 Day Readmissio NCT03034694 | Ohio State University | N/A |
| Completed | Effect of Teledermatology on Length of Hospital Admission, Length of Stay, 30 Day Readmission Rate, and Antibi NCT03036358 | Ohio State University | N/A |
| Completed | Predictors of Oral Antibiotic Treatment Failure in Emergency Department Patients With Cellulitis NCT02230813 | Royal College of Surgeons, Ireland | — |
| Completed | Comparing the Intravenous Treatment of Skin Infections in Children, Home Versus Hospital NCT02334124 | Murdoch Childrens Research Institute | N/A |
| Terminated | Duration of ANtibiotic Therapy for CEllulitis NCT02032654 | Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA) | Phase 4 |
| Terminated | Use of Corticosteroids in Children With Cellulitis NCT02087527 | Hospital General de Niños Pedro de Elizalde | N/A |
| Completed | Single Dose vs. Two Dose Regimen of Dalbavancin for the Treatment of Acute Bacterial Skin and Skin Structure I NCT02127970 | Durata Therapeutics Inc., an affiliate of Allergan plc | Phase 3 |
| Unknown | Continuous Regional Anesthesia for Septic Limb Orthopedic Surgery NCT01947660 | University Hospital, Strasbourg, France | N/A |
| Completed | Adjunctive Clindamycin for Cellulitis: C4C Trial. NCT01876628 | University Hospitals Bristol and Weston NHS Foundation Trust | Phase 4 |
| Completed | Optimising Diagnosis and Antibiotic Prescribing for Acutely Ill Children in Primary Care NCT02024282 | KU Leuven | N/A |
| Terminated | Sonographic Features of Cellulitis and Failure of Therapy NCT01773499 | University of Massachusetts, Worcester | — |
| Completed | Study Assessing Impact of Dermatology Consultation for Patients Admitted With Cellulitis NCT01706913 | Massachusetts General Hospital | N/A |
| Completed | Use of a Single Dose of Oral Prednisone in the Treatment of Cellulitis NCT01671423 | Albert Einstein Healthcare Network | N/A |
| Completed | The Effects of Daptomycin and Cytokines Production in Comparison With Vancomycin NCT01626560 | Hospital Universitario Evangelico de Curitiba | Phase 4 |
| Completed | Evaluation of Daptomycin for the Emergency Department Treatment of Complicated Skin and Skin Structure Infecti NCT01549613 | University of Cincinnati | Phase 4 |
| Completed | Soft Tissue Ultrasound of Infections NCT01557426 | Rhode Island Hospital | Phase 1 |
| Completed | A Phase 2 Safety and Exploratory Skin Lesion Measurement of TR-701 FA Study NCT01519778 | Trius Therapeutics LLC, a subsidiary of Merck & Co., Inc. (Rahway, New Jersey USA) | Phase 2 |
| Completed | A Study Assessing the Impact of Dermatology Consultation in Patients Presenting With Possible Cellulitis NCT01795092 | Massachusetts General Hospital | N/A |
| Completed | A Study of Safety, Tolerability, and Efficacy of AFN-12520000 in the Treatment of Acute Bacterial Skin and Ski NCT01519492 | Affinium Pharmaceuticals, Ltd | Phase 2 |
| Completed | Efficacy and Safety of Dalbavancin for the Treatment of Acute Bacterial Skin and Skin Structure Infections NCT01431339 | Durata Therapeutics Inc., an affiliate of Allergan plc | Phase 3 |
| Unknown | Far-IR Emitted by Compression Stockings for Cellulitis Treatment NCT01429428 | Federal University of São Paulo | N/A |
| Completed | Efficacy and Safety of Dalbavancin for the Treatment of Acute Bacterial Skin and Skin Structure Infections NCT01339091 | Durata Therapeutics Inc., an affiliate of Allergan plc | Phase 3 |
| Completed | Oritavancin Versus IV Vancomycin for the Treatment of Participants With Acute Bacterial Skin and Skin Structur NCT01252719 | Melinta Therapeutics, Inc. | Phase 3 |
| Completed | Oritavancin Versus IV Vancomycin for the Treatment of Patients With Acute Bacterial Skin and Skin Structure In NCT01252732 | Melinta Therapeutics, Inc. | Phase 3 |
| Completed | Comparison of Intravenous Cefazolin Plus Oral Probenecid With Oral Cephalexin for the Treatment of Cellulitis NCT01029782 | Kelowna General Hospital | Phase 2 |
| Withdrawn | The Use of Oral Steroids in the Treatment of Cellulitis NCT00893048 | Milton S. Hershey Medical Center | Phase 2 |
| Completed | Extracorporeal Shock Wave Treatment for Cellulite NCT01974115 | Concept-Clinic | N/A |
| Completed | Study of Wound Packing After Superficial Skin Abscess Drainage NCT00746109 | NYU Langone Health | Phase 4 |
| Completed | Procalcitonin Level and Kinetics in Children With Bacterial Infections NCT00714402 | Shaare Zedek Medical Center | — |
| Completed | Incision and Drainage Versus Needle Aspiration in Soft Tissue Abscesses NCT01085929 | University of Massachusetts, Worcester | Phase 3 |
| Completed | Cellulite and Magnetic Resonance Imaging NCT00636025 | Doris Hexsel | — |
| Completed | A Complicated Skin and Soft-tissue Infection Patient Registry NCT00737269 | Ortho-McNeil Janssen Scientific Affairs, LLC | — |
| Completed | Aquacel Versus Iodoform Gauze for Filling Abscess Cavity Following Incision and Drainage NCT00984022 | Valleywise Health | Phase 2 |
| Completed | A Study for Patients With Complicated Skin and Skin Structure Infections NCT00514527 | Targanta Therapeutics Corporation | Phase 2 |
| Unknown | Feasibility and Outcomes of Older Patients Hospitalization NCT00489021 | Hillel Yaffe Medical Center | N/A |
| Completed | Study of New Antibiotic Regimen for the Treatment of Uncomplicated Cellulitis in Emergency Department Patients NCT00676130 | Brigham and Women's Hospital | N/A |
| Completed | Study Comparing CUBICIN® (Daptomycin for Injection) With Vancomycin in Cellulitis or Erysipelas NCT00295178 | Cubist Pharmaceuticals LLC, a subsidiary of Merck & Co., Inc. (Rahway, New Jersey USA) | Phase 4 |
| Completed | An Attempt to Reduce Community-Acquired Methicillin-Resistant Staphylococcus Aureus (MRSA) Infection in Soldie NCT00289588 | Brooke Army Medical Center | N/A |
| Completed | Oral Moxifloxacin Versus Cefazolin and Oral Probenecid in the Management of Skin and Soft Tissue Infections in NCT00323219 | University of British Columbia | Phase 3 |
| Completed | Phase 2 Trial of TD 6424 (Telavancin) Versus Standard Therapy for Complicated Gram Positive Skin and Skin Stru NCT00061633 | Cumberland Pharmaceuticals | Phase 2 |
| Completed | Complicated Skin and Skin Structure Infections NCT00619710 | Pfizer | Phase 3 |
| Completed | Evaluation of Antibacterial Soap for Treatment of Lymphedema in a Filariasis-Endemic Area NCT00139100 | Centers for Disease Control and Prevention | N/A |
| Completed | A Study of the Safety and Effectiveness of Oral Levofloxacin Compared With Oral Ciprofloxacin in the Treatment NCT00257036 | Johnson & Johnson Pharmaceutical Research & Development, L.L.C. | Phase 2 / Phase 3 |
| No Longer Available | Direct Antibiotic Delivery of Cefazolin Into Soft Tissue Infections Using Subcutaneous Injection and Ultrasoni NCT01238276 | Sonescence, Inc. | — |