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Research Article

Clinical efficacy and safety of trimonthly administration of goserelin acetate 10.8 mg in premenopausal Chinese females with symptomatic adenomyosis: a prospective cohort study

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Article: 2160435 | Received 06 Jul 2022, Accepted 14 Dec 2022, Published online: 23 Dec 2022

Figures & data

Figure 1. Patient disposition.

Figure 1. Patient disposition.

Table 1. Baseline patient demographics and disease characteristics.

Figure 2. Dysmenorrhea scores from baseline to 12 weeks in goserelin 10.8 mg and 3.6 mg groups, 12 weeks vs baseline p < .0001.

Figure 2. Dysmenorrhea scores from baseline to 12 weeks in goserelin 10.8 mg and 3.6 mg groups, 12 weeks vs baseline p < .0001.

Figure 3. Uterine volume from baseline to 12 weeks in goserelin 10.8 mg and 3.6 mg groups, 12 weeks vs baseline p < .0001.

Figure 3. Uterine volume from baseline to 12 weeks in goserelin 10.8 mg and 3.6 mg groups, 12 weeks vs baseline p < .0001.

Figure 4. CA125 from baseline to 12 weeks in goserelin 10.8 mg and 3.6 mg groups, 12 weeks vs baseline p < .0001.

Figure 4. CA125 from baseline to 12 weeks in goserelin 10.8 mg and 3.6 mg groups, 12 weeks vs baseline p < .0001.

Figure 5. HGB from baseline to 12 weeks in goserelin 10.8 mg and 3.6 mg groups, 12 weeks vs baseline p < .0001.

Figure 5. HGB from baseline to 12 weeks in goserelin 10.8 mg and 3.6 mg groups, 12 weeks vs baseline p < .0001.

Table 2. Treatment outcomes in goserelin 10.8 mg and goserelin 3.6 mg groups.

Table 3. Incidence of adverse events occurring in goserelin 10.8 mg and 3.6 mg groups.