The Effect of an Iranian Herbal Drug on Primary Dysmenorrhea: A Clinical Controlled Trial

Authors

  • Khodakrami Nahid MSM,

    Corresponding author
    1. Khodakrami Nahid, MSM, is a lecturer in the Midwifery Department at the Nursing Midwifery School and Reproductive Health research center, Shahid Beheshti Medical University, Tehran, Iran.
      Shahid Beheshti Medical University, Reproductive Health Research Center, Nursing Midwifery School, Tehran, Iran. E-mail: khodakarami@sbmu.ac.ir
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  • Moatar Fariborz PhD,

    1. Moatar Fariborz, PhD, is a professor in the Department of Pharmacognosy at the Isfahan Medical University, Isfahan, Iran.
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  • Ghahiri Ataolah MD,

    1. Ghahiri Ataolah, MD, is an Associate Professor in the Department of OB/Gyn at the Alzahra Teaching Hospital, Isfahan Medical University, Isfahan, Iran.
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  • Shahdan Solokian MS

    1. Shahdan Solokian, MS, is a lecturer at the Farzanegan Amin School and Khorasgan Azad University, Isfahan, Iran.
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Shahid Beheshti Medical University, Reproductive Health Research Center, Nursing Midwifery School, Tehran, Iran. E-mail: khodakarami@sbmu.ac.ir

Abstract

Our objective was to examine the effect of an Iranian herbal drug in the treatment of primary dysmenorrhea. A randomized, double-blind, placebo-controlled pilot trial among 180 female students at Isfahan University dormitory aged 18 to 27 who suffered from primary dysmenorrhea was undertaken. The participants were randomly divided into three groups: herbal drug, mefenamic acid, and placebo. The herbal drug group was given 500 mg of highly purified saffron, celery seed, and anise (SCA) extracts three times a day for three days, starting from the onset of bleeding or pain. Participants were followed for two to three cycles from the beginning of menstruation through the three days of bleeding. Main outcome measures were the severity and duration of pain at 2 and 3 months. A visual analogue scale was used to record pain. There were statistically significant reductions in pain scores and pain duration scores in the groups that took SCA (P < .001) and mefenamic acid (P < .01). The decrease in pain score was reflected by a significant reduction in other drug use among the treatment groups compared with the women in the placebo group. The magnitude of the reduction was significantly greater in the SCA group than in the mefenamic acid and placebo groups. Both drugs effectively relieved menstrual pain as compared with the placebo. More clinical trials are needed to establish the efficacy of this herbal drug.

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