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Table 3 Characteristics and outcomes of the included studies

From: Outcome assessment methods of bioactive and biodegradable materials as pulpotomy agents in primary and permanent teeth: a scoping review

  

Mean (SD)

Sample size

 

84.9 (71.6)

  

n (%)

Study design

 
 

Randomized controlled trial

107 (84.3%)

 

Non-randomized trial

20 (15.7%)

Follow-up duration

 
 

Less than 6 months

5 (3.9%)

 

6 months

11 (8.7%)

 

9 months

2 (1.6%)

 

12 months

61 (48%)

 

More than 1 year

48 (37.8%)

Outcome measured

 

Clinical and radiographic

115 (90.6%)

 

Clinical, radiographic and histological

7 (5.5%)

 

Histological

2 (1.6%)

 

Clinical, radiographic and inflammatory

1 (0.8%)

 

Histological and immunohistochemistry

1 (0.8%)

 

Clinical, radiographic and microbiological

1 (0.8%)

Primary/permanent teeth

 
 

Primary teeth

86 (67.7%)

 

Permanent teeth

 
 

Mature teeth

29 (22.8%)

 

Immature teeth

12 (9.4%)

Pulp exposure type

 
 

Carious

114 (89.8%)

 

Traumatic

6 (4.7%)

 

Carious or traumatic

4 (3.1%)

 

Sound tooth indicated for extraction

3 (2.4%)

Pre-operative pulp status

 

Normal pulp

5 (3.9%)

 

Reversible pulpitis

104 (81.9%)

 

Irreversible pulpitis

13 (10.2%)

 

Reversible or Irreversible pulpitis

3 (2.36%)

 

NOT MENTIONED

2 (1.57%)