Abstract

Objective To evaluate the efficacy and safety of aceclofenac–drotaverine combination against aceclofenac alone in patients with primary dysmenorrhoea. Study design This double-blind, double-dummy, randomized, comparative, multicentric study enrolled 200 women (100 women in each arm) in the age range of 18–35 years with primary dysmenorrhoea at four centers. The patients were randomly allocated to either aceclofenac 100 mg–drotaverine 80 mg b.i.d or aceclofenac 100 mg alone b.i.d for a maximum of 3 days. Primary efficacy parameters were total area under pain relief (PR) score up to 4 and 8 h (TOPAR/4 and TOPAR/8). Secondary efficacy measurements were pain-intensity difference (PID), sum of PID over 4 and 8 h (SPID/4 and SPID/8), peak PID over 4 and 8 h and peak PR over 4 and 8 h, total study drug consumption, and patient's and investigator's global evaluation of the efficacy. Results Both treatments showed significant improvement in baseline values in all efficacy parameters. The combination was significantly superior to monotherapy in terms of TOPAR/4 (24.0 vs 18.54) ( p = 0.000) and TOPAR/8 (40.3 vs 35.2) ( p = 0.003), SPID/4 (−17.9 vs −13.88) ( p = 0.000) and SPID/8 (−31.06 vs −26.8) ( p = 0.001), peak PID/4 (−6.60 vs −5.75) ( p = 0.001) and peak PR/4 (8.26 vs 7.10) ( p = 0.000). At the end of 8 h, both treatments were comparable with respect to peak PID/8 and peak PR/8 ( p > 0.05). The total number of doses consumed by patients treated with combination therapy was less than with monotherapy (150 vs 168 doses). The combination was significantly superior to monotherapy with respect to patient's and investigator's global evaluation of the efficacy ( p = 0.002 and p = 0.001, respectively). Both treatments were well tolerated. Conclusion This study establishes the efficacy of aceclofenac–drotaverine combination in patients with primary dysmenorrhoea. The fixed-dose combination of aceclofenac and drotaverine should therefore be considered as a suitable, effective and well tolerated treatment option for primary dysmenorrhoea.

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