I've gotten reliable results with SYBR-green based assays for miRNAs that are mid-high in abundance. I used a poly A tailing method to make the cDNA which had a universal primer as a "forward" sequence.
However, if you can afford it and don't know how primer design works, I'd say Taqman is a safer way. Taqman will also be more sensitive to differentiating between closely-related family of miRNAs that are nearly identical in sequence.
So for the easy stuff, go with custom primers + SYBR green, hard stuff Taqman.
Well both will give you results, however Taqman qPCR provides you with more Specificity and Reproducibility. Please check the following link: http://www.thermofisher.com/de/de/home/life-science/pcr/real-time-pcr/real-time-pcr-learning-center/real-time-pcr-basics/taqman-vs-sybr-chemistry-real-time-pcr.html
If you needed a help in anything, please let me know. Best of luck to you!