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The aim of this study is to correlate time to achieve haemostasis and concentration of IL-8 in pulpal blood to the outcome of partial pulpotomy after 3 and 6 months follow up.

Not Applicable
Conditions
Health Condition 1: K040- Pulpitis
Registration Number
CTRI/2023/06/054485
Lead Sponsor
Dr Saada Sulaiman
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

< 45 years of age

non-contributory medical history

Deeply carious permanent molar with a preoperative provisional diagnosis of symptomatic irreversible pulpitis.

History of spontaneous pain and nocturnal pain which aggravates on lying down.

No history and signs of sinus tract, pus exudate, fistula, clinical swelling.

Spontaneous pain and/or with sharp and lingering pain upon cold testing using Endo-Ice.

Restorable tooth with probing pocket depth ( <3mm)

Tooth mobility within normal limits

Complete caries excavation would likely result in pulpal exposure.

Haemorrhage from the pulp exposure site stops with NaOCl placement within 15 minutes.

The radiolucent caries penetrating the entire thickness of the dentine (extremely deep caries).

Absence of periapical or furcation changes in the radiograph.

Exclusion Criteria

1)Unexposed pulp after complete caries excavation.

2)Uncontrolled pulpal haemorrhage during the procedure lasting more than 15 minutes.

3)Absence of bleeding after pulp exposure; the pulp is judged as necrotic or partially necrotic.

4)Tooth showing negative response to cold testing or presence of sinus tract or swelling.

5)Non-restorable teeth with cracks or subgingival caries, associated sinus or swelling.

6)Tooth with poor periodontal support.

7)Prominent radiolucency at the furcation or periapical regions.

8)Presence of Immature root apices/ apical resorption.

9)Presence of internal or pathologic external root resorption, calcification or pulp canal obliteration.

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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