Table 2.
The basic characteristics of the excluded published articles and participants.
| Study ID | Study duration | Reason of exclusion | Study arms | N | Main results |
|---|---|---|---|---|---|
| Jayne 2012[26] | 52 weeks | - Open-label extension study of previous 5 clinical trials. - Had no placebo arm. |
Flibanserin 50–100 mg/d | 1723 | - Somnolence, sedation, fatigue, dizziness, nausea, and vomiting were reported by 15.8%, 1.6%, 7.6%, 6.9%, 6.3%, and 1.4% of participants, respectively. - At study end, 42% of baseline non-remitters had improved their FSFI score to remission level. |
FSFI = Female Sexual Function Index.