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Table 3 Variables for Secondary End Points and Adverse Events in each Group

From: The efficacy and safety of indocyanine green-hyaluronic acid mixture (LuminoMark™) for localization in patients with non-palpable breast lesions: a multi-center open-label parallel phase-2 clinical trial

 

Control group

(n = 14)

Test Group 1

(n = 15)

Test Group 2

(n = 15)

p-value

Marking on breast lesion

Yes

13 (92.9%)

13 (86.7%)

14 (93.3%)

0.954

No

1 (7.1%)

2 (13.3%)

1 (6.7%)

 

Marking on excised specimen

Yes

13 (92.9%)

14 (93.3%)

15 (100.0%)

0.357

No

1 (7.1%)

1 (6.7%)

0 (0.0%)

 

Skin pigmentation

    

Yes

9 (64.3%)

0 (0.0%)

0 (0.0%)

0.000

No

4 (28.6%)

15 (100.0%)

15 (100.0%)

 U

Unknown

1 (7.1%)

0 (0.0%)

0 (0.0%)

 

Histopathological accuracy

Mean (±sd)

0.3 (±0.1)

0.4 (±0.1)

0.4 (±0.1)

0.331(group1-2)

0.389(group2-3)

0.914(group1-3)

Adverse events (AEs)

Yes

0(0.0%)

0(0.0%)

0(0.0%)

1.000

No

14(100.0%)

15(100.0%)

15(100.0%)

 
  1. sd standard deviation