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1.
Clin Rheumatol ; 18(1): 4-9, 1999.
Article in English | MEDLINE | ID: mdl-10088941

ABSTRACT

In this multicentre (five centres in Germany), randomised, double-blind, comparative study, 150 patients with painful degenerative joint disease according to EULAR criteria received either oxaceprol (200 mg three times daily) or diclofenac (25 mg three times daily) for 20 days. Joint function, the primary variable, assessed according to Lequesne's indices, improved equally in both treatment groups to a clinically relevant degree. Joint mobility improved by approximately 60% in both groups. By the end of therapy in both groups, the period of pain-free walking time had more than doubled and subjectively evaluated pain perception (VAS) was reduced by almost 50% without any significant differences between the treatments. The incidence of adverse drug reactions was similar in both groups but oxaceprol induced milder symptoms. Oxaceprol is as effective and better tolerated than diclofenac in the treatment of osteoarthritis.


Subject(s)
Anti-Inflammatory Agents, Non-Steroidal/therapeutic use , Diclofenac/therapeutic use , Hydroxyproline/analogs & derivatives , Osteoarthritis, Hip/drug therapy , Osteoarthritis, Knee/drug therapy , Administration, Oral , Adult , Aged , Aged, 80 and over , Anti-Inflammatory Agents, Non-Steroidal/administration & dosage , Arthralgia/drug therapy , Arthralgia/etiology , Diclofenac/administration & dosage , Double-Blind Method , Female , Follow-Up Studies , Humans , Hydroxyproline/administration & dosage , Hydroxyproline/therapeutic use , Male , Middle Aged , Osteoarthritis, Hip/complications , Osteoarthritis, Hip/physiopathology , Osteoarthritis, Knee/complications , Osteoarthritis, Knee/physiopathology , Pain Measurement , Range of Motion, Articular , Safety , Treatment Outcome
2.
Z Orthop Ihre Grenzgeb ; 120(3): 343-7, 1982.
Article in German | MEDLINE | ID: mdl-7113376

ABSTRACT

On account of 41 cases of spondylolisthesis a one-stage operation for repositioning and stabilisation using Harrington's instrumentation with anterior intercorporal spine fusion is recommended. The advantage of this procedure is a secure fusion and a short hospitalisation. After 6 months the patient usually is rehabilitated.


Subject(s)
Spinal Fusion/methods , Spondylolisthesis/surgery , Traction/methods , Adolescent , Adult , Biomechanical Phenomena , Female , Humans , Male , Middle Aged , Outcome and Process Assessment, Health Care , Postoperative Complications/diagnostic imaging , Radiography , Spinal Fusion/instrumentation , Spondylolisthesis/diagnostic imaging
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