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They sit near the top of the evidence hierarchy, just below meta-analyses (which combine multiple RCTs)

extracellular matrix signalling

There are also no validated dosing guidelines for DSIP, which compounds the risk: an unvalidated dose paired with a product of unverified identity is a poor foundation for any clinical decision

The clinical decision on protocol length and maintenance frequency is made at the APRN evaluation based on the individual patients response and goals

Legal Status of DSIP DSIP, like many experimental peptides, sits in a regulatory gray zone