Table 1.
Study | Details of hormone administration | RCT study | Follow-up | Jadad score | |
---|---|---|---|---|---|
HRT group | Control group | ||||
Guaschino et al.,2003 [6] | Equine conjugated estrogens 0.625 mg/day and dydrogesterone 5 mg/day in a continuous combined regimen; no ophthalmic treatment. | No hormonal or ophthalmic treatment. | Yes | 1 year | 3 |
| |||||
Erdem et al., 2007 [14] | Conjugated estrogen 0.625 mg/day and medroxyprogesterone acetate 5 mg/day in a continuous combined regimen; no dry eye medication was given. | No hormone. Artificial tear products were allowed. | No | 3 months | 0 |
| |||||
Affinito et al., 2003 [7] | Transdermal 17β-estradiol (E2), 50 µg/day, and medroxyprogesterone acetate 10 mg/day for 12 days per cycle. | No hormonal or ophthalmic treatment. | Yes | 3 months and 6 months | 4 |
| |||||
Taner et al., 2004 [15] | Estradiol plus medroxyprogesterone acetate (Premelle 5 mg), one tablet, qid. | No hormonal or ophthalmic treatment. | No | 6 months | 0 |
| |||||
Scuderi et al., 2012 [13] | Phytoestrogen, one tablet, bid for 1 month; artificial tear products were allowed. | Placebo tablet. Artificial tear products were allowed. | Yes | 1 month | 6 |
Scuderi et al., 2012 [13] (reversed group) |
Lacrisek tablet. Each Lacrisek tablet contained α-lipoic acid (100 mg), eicosapentaenoic acid (240 mg), and extract of fenugreek (200 mg), which contains diosgenin (1.3%), steroidal saponins (50%), and alkaloids; artificial tear products were allowed. |
HRT: hormone replacement therapy; RCT: randomly controlled trial.