“…Seventeen of these studies required that patients objectively lose greater than 80 milliliters menstrual blood loss per cycle in order to be eligible for study participation. [10-15, 18-23, 25-29] Five studies included a levonorgestrel intrauterine system arm [15, 20, 22, 26, 27], 5 studies included a OCP arm [15, 16, 21, 27, 29], 5 studies included a luteal progestin arm[8, 11, 19, 22, 25], 1 study included an extended oral progestin arm[20], 8 studies included an NSAID arm[9, 11-13, 16-18, 36], 7 studies included an antifibrinolytic arm (tranexamic acid, tranexamic acid prodrug, or epsilon amino caproic acid) [9, 10, 14, 23-25, 28]. Studies ranged in quality, and the quality of individual studies are noted in Table 1.…”