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. 2020 Jun 30;11(2):e2. doi: 10.5037/jomr.2020.11202

Table 4.

Injection protocol and administration

Study Group Injection

Injection protocol Administration of injections
Wu et al. [27] BT-A 75 U (1.5 mL) of BT-A were applied at 15 points, 5 U (0.1 mL) per point in trigger points Intradermally and/or submucosally

Placebo

Shehata et al.
[28]
BT-A Every patient received either BT-A (100 U BOTOX® in 2 mL preservative-free normal saline, resulting in a concentration of 5 units/0.1 mL) or placebo (2 mL 0.9% NaCl).
Overall injected doses ranged from 40 units (8 injection points) to 60 units (12 points)
Subcutaneously

Placebo

Zúñiga et al. [29] BT-A A 1 mL syringe: 0.9% saline plus 50 U of BT or only 1 mL of 0.9% saline were administered in various sites,
1 cm apart from one another in the path of the branch/branches involved.
Subcutaneously

Placebo

Zhang et al. [30] BT-A (25 U) BT-A or the same volume of isotonic saline were applied at 20 points, (0.05 ml) per point,
between the epidermis and dermis of the skin where pain was experienced according to the patient's description.
Intradermally
and/or submucosally

BT-A (75 U)

Placebo

U = units per ml of solution; BT-A = botulinum toxin type A; TN = trigeminal neuralgia.