M80 M81 M82
Conditions
Interventions
Group 1: Oscarvit, 3x600 mg/day, for 20 days
Sponsors
Universitätsklinikum Schleswig Holstein, Hals-,Nasen-,Ohrenklinik, Kopf- und Halschirurgie
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: The patient is suffering from osteoporoses/osteoarthrosis
Exclusion criteria
Exclusion criteria: There is no participation for patients who are not suffering from osteoporoses/osteoarthrosis
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| After 20 days treatment with OSC (3x600mg/day) the alleviation of pain will be measured by questioning of the patients in accordance with Numeric Pain Rating Scale (NPRS). | — |
Secondary
| Measure | Time frame |
|---|---|
| Additional goal criteria for the study was the evaluation of pain after 5- and 10 days treatment with OSC according to NPRS. | — |
Countries
Germany
Contacts
Public ContactTibor Görögh
Universitätsklinikum Schleswig-Holstein Hals-,Nasen-,Ohrenklinik, Kopf- und Halschirurgie
Outcome results
None listed