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 |