DRKS00028473
Not yet recruiting
Phase 4
Functional outcome and painrelief in patients with osteoarthritis of the knee due to oral intake of UC II (undenaturated collagen Typ II):A multicenter, prospective, randomised, placebo controlled clinical trial - OIUC2
Orthopädie im MediaparkMediaPark Klinik Köln0 sites202 target enrollmentMarch 9, 2022
Overview
- Phase
- Phase 4
- Intervention
- Not specified
- Conditions
- M17.1
- Sponsor
- Orthopädie im MediaparkMediaPark Klinik Köln
- Enrollment
- 202
- Status
- Not yet recruiting
- Last Updated
- last year
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Sufficiently severe gonarthrosis grade II and III according to the nativradiological criteria according to Kellgren/Lawrence or magnetic resonance imaging criteria according to Outerbridge.
- •Diagnosis confirmed by standard X\-ray (AP, lateral, patella tangential, Rosenberg, whole leg) or MRI
- •Age: 50\-70 years
- •Gender: both
Exclusion Criteria
- •Exclusion criteria (knee\-related)
- •\- Arthrofibrosis
- •\- Extension deficit (\<20°)
- •\- Flexion deficit (\> 100°)
- •\- Insufficiency of the anterior and/or posterior cruciate ligament
- •\- Intra\-articular injections with corticosteroid, hyaluronic acid and PRP in the last 3 months
- •\- Chronic use of medication with effect on the joint (e.g. corticoid)
- •Exclusion criteria (not knee related)
- •\- Insufficient German language skills
- •\- Immunological diseases / autoimmune diseases / rheumatic disease
Outcomes
Primary Outcomes
Not specified
Similar Trials
Completed
Not Applicable
Pain and patient-reported outcome associated with surgery for carpal tunnel syndrome or trigger finger under local anesthesia with and without tourniquetNL-OMON48016Jeroen Bosch Ziekenhuis142
Completed
Not Applicable
ong-term results of pain therapy in patients with CRPS compared to patients with neuralgia and post-traumatic joint pain as a control group - telephone interview 1-5 years after initiation of therapyG56G57M89Mononeuropathies of upper limbMononeuropathies of lower limbOther disorders of boneDRKS00013930Abteilung für Schmerzmedizin Berufsgenossenschaftliches Universitätsklinikum Bergmannsheil gGmbH Bochum359
Active, not recruiting
Not Applicable
Patient-reported and functional outcomes following ReActiv8 implantable neurostimulatioACTRN12622000555752BackSpace Clinics Pty Ltd.50
Recruiting
Not Applicable
Debridement vs debridement and biodegradable ballooShoulder debridement biodegradable balloon rotator cuff tear Schouder debridement , bio-oplosbare ballon, rotator cuff herstelNL-OMON24952Afdeling OrthopaedieHAGA HospitalSportlaan 6002566MJ, Den Haag, Nederland104
Recruiting
Not Applicable
Difference in pain and functional outcome after arthroscopic debridement vs. debridement and biodegradable implanted balloon for irreparable rotator cuff tears.irreparable rupture of the muscles around the shouldermassive rotator cuff tears1004323710041297NL-OMON50270Reinier Haga Orthopedisch Centrum104