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Abstract
In a randomized, double-blind, parallel-group, multicenter study, the efficacy and
tolerability of diclofenac dispersible were compared with placebo in the treatment
of acute soft-tissue injuries. Patients seen within 48 hours of a soft-tissue injury
received either diclofenac dispersible 50 mg or placebo three times daily for 3 to
7 days, with paracetamol allowed as a rescue analgesic. Of a total of 253 recruited
patients, 247 patients (122 in the diclofenac dispersible group and 125 in the placebo
group) were eligible for tolerability assessment and 229 patients (115 diclofenac
dispersible and 114 placebo) were eligible for efficacy analysis. In the general,
median reductions in the intensities of pain at rest, on movement, and on local pressure
(as measured on 100-mm analog chromatic continuous scales) were greater with diclofenac
dispersible than with placebo after treatment (differences did not reach statistical
significance). At the center that recruited the largest number of patients, the initial
median levels of pain at rest and on movement were considerably lower than those at
the other centers. On reanalysis of the pain data without this center, a significant
difference favoring diclofenac dispersible over placebo was noted for pain on movement
and on local pressure (P ≤ 0.044). With respect to daily assessment of pain severity, more patients in the
diclofenac dispersible group had none or mild pain while fewer had moderate or severe
pain during the early posttreatment days; this treatment difference versus placebo
reached statistical significance on days 3 and 4 (P ≤ 0.045). Nine (7.4%) of 122 patients in the diclofenac dispersible group reported
adverse events, compared with 11 (8.8%) of 125 patients in the placebo group. Gastrointestinal
complaints predominated in both groups, but severe diarrhea (4 patients) was reported
with diclofenac dispersible only. We concluded that drinkable diclofenac dispersible
provides effective relief of moderate-to-severe pain in the early stages of acute
soft-tissue injury. In addition, the drug is well tolerated when used short-term for
treatment of such injuries.
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© 1995 Published by Elsevier Inc.