KCT0006745
Recruiting
未知
Pilot study to evaluate the efficacy and safety of MegaNuovo in Pressure sore patients : single center, comparative, investigator-initiated pilot study
Yonsei University, Wonju Severance Christian Hospital0 sites30 target enrollmentTBD
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Diseases of the skin and subcutaneous tissue
- Sponsor
- Yonsei University, Wonju Severance Christian Hospital
- Enrollment
- 30
- Status
- Recruiting
- Last Updated
- 4 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •? Patients aged 19 to less than 90 years of age
- •? Patients with stage 2\~4 pressure ulcers
- •? Patients who have fully explained the purpose and contents of the test before taking the test and voluntarily signed the written consent (a legal representative can represent him if necessary)
- •? Patients who can follow\-up during the test period
Exclusion Criteria
- •? HbA1c\=12%
- •? Patients with evidence of active infection including osteomyelitis or cellulitis
- •? Patients who want surgical treatment
- •? Pregnant and lactating women (urine hCG test)
- •? Patients with psychiatric problems
- •? Patients with infectious diseases, systemic autoimmune diseases (rheumatic diseases, etc.), blood clotting disorders (diagnosed by medical staff through questionnaire and physical examination)
- •? In case it is judged difficult to conduct clinical trials by the principal investigator
Outcomes
Primary Outcomes
Not specified
Similar Trials
Active, not recruiting
Phase 1
Pilot study to evaluate the efficacy and safety of mefloquine as prophylaxis in people exposed to the disease caused by the new SARS-CoV-2 coronavirus (COVID-19)COVID-19 infection is being spread around the world with more than 400.000 cases. The spred of the disease is being a world health problem.Therapeutic area: Diseases [C] - Virus Diseases [C02]EUCTR2020-001194-69-ESFélix Gutiérrez Rodero200
Completed
Not Applicable
Safety and efficacy of Transcend CyPass glaucoma implant in open angle glaucoma patients who have failed medical treatmentPrimary open angle glaucomaEye DiseasesGlaucomaISRCTN23263504Transcend Medical, Inc.™ (USA)20
Completed
Not Applicable
Transcend CyPass glaucoma implant and cataract surgery in open angle glaucoma patientsISRCTN86839890Transcend Medical, Inc.™ (USA)20
Active, not recruiting
Not Applicable
A pilot study to assess the efficacy and safety of LCQ908 alone and in combination with fenofibrate or Lovaza® in patients with severe hypertriglyceridemiaon Familial Chylomicronemia Syndrome (Non-FCS)MedDRA version: 14.1Level: LLTClassification code 10020870Term: HypertriglyceridemiaSystem Organ Class: 10027433 - Metabolism and nutrition disordersTherapeutic area: Diseases [C] - Nutritional and Metabolic Diseases [C18]Non Familial Chylomicronemia Syndrome (Non-FCS)EUCTR2012-000872-40-CZovartis Pharma Services AG60
Completed
Phase 3
A pilot study to assess the efficacy and safety of Heliox inhalation therapy for resuscitation to preterm infants.preterm infantsJPRN-UMIN000015061agano Children's Hospital10