Acute pain and Chronic pain
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1.Men and women between the ages of 20 and 80 years old. 2.Patients with pain symptoms in the following areas Neck. Shoulder joint. Knee joint Lower back. Ankle joint (including foot) 3.Patients who have given written consent to participate in the study
Exclusion criteria
Exclusion criteria: 1. Patients who have taken anti-inflammatory analgesics within 8 hours prior to the administration of the study drug 2. Patients who have used sleeping pills, psychotropic drugs, or other psychiatric drugs within 24 hours prior to administration of the study drug 3. Patients suffering from infectious diseases 4. Patients with a history of cancer or active malignancy 5. Patients with hypoglycemic symptoms prior to administration of the study drug 6. Patients who are judged to be inappropriate as research subjects by the principal investigator and principal study investigator
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Perform pain and functional assessment prior to administration of the study drug, pain and functional assessment 30 minutes after administration, pain and functional assessment 24 hours after administration, pain and functional assessment 7days after administration,pain and functional assessment 14 days after administration | — |
Countries
Japan
Contacts
General incorporated association Advalife Science SINCLAIR GINZA CLINIC Nursing Deptment