| Literature DB >> 34290964 |
Zahra Niazi Mashhadi1, Morvarid Irani2,3, Mahin Kiyani Mask2,3, Clara Methie4.
Abstract
OBJECTIVE: During recent years, evidence-based practice as a way to support higher standards of care was emphasized by health care policymakers. Sexual dysfunction (SD) is a common problem that affects the quality of life in individuals. Today, the use of Ginkgo biloba extract (GBE) for treating SD has been considered, so this study was performed to evaluate the current evidence for the efficacy and safety of ginkgo in treating SD.Entities:
Keywords: Complementary and alternative medicine; Ginkgo (Ginkgo biloba) Systematic review; Sexual dysfunction
Year: 2021 PMID: 34290964 PMCID: PMC8264219 DOI: 10.22038/AJP.2021.17813
Source DB: PubMed Journal: Avicenna J Phytomed ISSN: 2228-7930
Figure 1PRISMA flow diagram of article selection progress
Summary of randomized clinical trials that tested Ginkgo biloba effects on sexual function
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| Malakouti et al. | 6 weeks | 45 |
| placebo | N=60 | N=60 | N=116 | 3% | female sexual function index (FSFI) | double blind | The average of total sexual function scores in | Nausea, Abdomen pain, Headache, Gripe |
| Amiri et al. | One | 50 |
| placebo | N=40 | N=40 | N=63 | 21.2 % | the Sabbatsberg Sexual Rating Scale | triple-blind | Significant improvements in sexual desire were observed after consuming | Without any side effects |
| Meston et al. | 8 weeks | 18 |
| placebo | N=134 | N=16 | N=127 | 5.2% | the Female Sexual Function Index (FSFI), | double-blind | Long-term GBE intervention did not significantly difference in arousal responses with placebo. 1) None of the short-term and long-term GBE alone showed any significant effect after the intervention.2) Also observed a significant effect in the placebo group in women with sexual concerns. | Not reported any side effects for ginkgo biloba |
| Wheatley, | 12 weeks | 18 |
| placebo | N=11 | N=13 | N=21 | 12.5% | Sexual problems questionnaire (A new scale) | Triple-blind | From week 0 to week 6, no significant difference were found in any of the intervention groups.The non-blind follow-on period of another 6 weeks was completed by 6 participants on placebo and 7 on | Had to omit- Gastric pain/nausea- ‘Muzzy head’- Anaesthesia/paraesthesia fingers and palpitations |
| Kang et al. | Two | 45 |
| placebo | N=19 | N=18 | N=25 | 32% | questionnaire | double-blind | No significant changes were found in any of the items related to sexual function at premedication or in the 2td and 4th weeks after intervention. After 8 weeks of intervention, only in one item (orgasm) were significantly difference found and even in the case of this item, the placebo group showed significant difference. | Gastrointestinal disturbance, Sedation ,headache , Increased oral intake |
Methodological assessment of study quality by Oxford Center for Evidence-Based Medicine checklist
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| 1 | 2 | |||||||
| 1 | Jamileh Malakouti et al. (2017) | + | - | + | + | + | + | + |
| 2 | Amiri Mina et al. (2014), Iran | + | + | + | + | + | + | + |
| 3 | Cindy M. Meston et al. (2008) | + | + | + | + | + | + | - |
| 4 | David Wheatley et al. (2004) | + | + | + | + | + | + | - |
| 5 | Byung-JoKang et al. (2002), South Korea | + | + | + | + | + | + | - |