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. 2021 Nov 25;2021:8967219. doi: 10.1155/2021/8967219

Table 3.

Methodology assessment.

Author and year Microbial inoculation Root canal preparation (instruments used and size of preparation) Irrigation protocol Volume of irrigant Time of irrigation Needle used for irrigation Irrigant activation devices used
Ok et al. 2015 [5] E. faecalis (ATCC 29212) cultured in a BHI agar suspension adjusted to 1 × 108 CFU ProTaper NiTi rotary files 30.06% taper No protocol mentioned 6 ml of each irrigant 2 min Not mentioned in the study Nil
Pujar et al. 2011 [11] E. faecalis cultured in a BHI agar (strain not mentioned) Step back upto 40 K file No protocol mentioned 3 ml of each irrigant 10 mins Not mentioned in the study Nil
Choudhary et al. 2018 [12] E. faecalis (MTCC 2729) and C. albicans (MTCC 1637) in a BHI agar is inoculated in 5 mL of suspension to obtain 1 : 1010 dilution Step back upto 40 K file During canal preparation, 3 mL of respective irrigant was used for 15 mins after enlargement, 2 mL of irrigant solution was used to rinse debris in the canals for another 5 min. Sterile normal saline (2 mL) was used as a final rinse 5 ml of each irrigant 20 mins 30-gauge needle Nil
Sedigh-Shams et al. 2015 [13] C. albicans in sabouraud dextrose agar suspensions adjusted to 1.5 × 108 CFU ProTaper NiTi rotary files 30.06% taper During canal preparation, 10 ml of respective irrigants were used. Groups 1 and 2 were irrigated with 2 ml of sterile distilled water to remove the remaining Z. multiflora EO. Group 3 were irrigated with 2 ml of 4% sterile sodium thiosulfate solution to neutralize the remaining NaOCl 10 ml of each irrigant 12–14 mins 27-gauge needle Nil
Rosaline et al. 2013 [14] E. faecalis (ATCC 29212) cultured in tryptone bile X-glucuronide agar suspensions adjusted to 1 × 106 cells/ml Not mentioned in the study All the specimens were treated with 5.25% NaOCl for 30 min followed by 5 mmol/L 17% EDTA for 5 mins. After which, the final irrigants were used Not mentioned about the volume of final rinse Final irrigation for 30 mins Not mentioned in study Nil
Gupta–Wadhwa et al. 2016 [15] E. faecalis (ATCC 29212) suspensions adjusted to 1.5 × 108 CFU ProTaper NiTi rotary files 30.06% taper Initially, 2 mL of experimental extract for 30 s; during instrumentation, the canal was irrigated with 2 mL of the tested extract. After instrumentation experimental, extract was left undisturbed for 60 s and then finally irrigated with 2 mL of 3% NaOCl followed by 5 mL of 17% EDTA for 1 min and again with 2 mL of experimental extract 20 ml used in each canal 6mins 30 s approx. 30-gauge needle Nil
Sharifian et al. 2009 [16] E. faecalis (ATCC 29212) Specimens enlarged low-speed round burs of ISO sizes 025, 027, 029, 031, and 033 No protocol was mentioned Not mentioned 20 mins contact time of irrigant Not mentioned Nil
Divia et al. 2018 [17] E. faecalis (ATCC 29212) Step back upto 50 k file No protocol was mentioned Not mentioned Not mentioned Not mentioned Nil
Kumar et al. 2018 [18] E. faecalis (strain not mentioned) Step back up to 30K size No protocol was mentioned 6 ml of irrigants At the rate of 2 ml/15 seconds 25-gauge needle Nil