Skip to main content
Clinical Trials/CTRI/2025/04/085860
CTRI/2025/04/085860Not yet recruitingPhase 2/3

Evaluation of vital pulp therapy in permanent teeth with irreversible pulpitis using different materials an in vivo study

Government Dental College and hospital Ahmedabad1 site in 1 country60 target enrollmentStarted: May 16, 2025Last updated:
Conditions

Trial Snapshot

Phase
Phase 2/3
Status
Not yet recruiting
Sponsor
Enrollment
60
Locations
1
Primary Endpoint
Absence of pain and discomfort except during the first week after treatment

Study Overview

Brief Summary

AIM :TO EVALUATE THE EFFICACY OF CHITOSAN ANDSODIUM HYPOCHLORITE AS HEMOSTATIC AGENTS IN REDUCING POST OPERATIVE PAIN AND TOASSESS SEALING ABILITY AND HEALING OUTCOMES OF DIFFERENT MEDICAMENTS IN CASESOF IRREVERSIBLE PULPITIS UNDERGOING PULPOTOMY PROCEDURE IN PERMANENT TEETH .

OBJECTIVES:

•Toevaluate and compare efficacy of chitosan and sodium hypochlorite ashaemostatic agents in reducing post operative pain following pulpotomy inpermanent teeth with irreversible pulpitis.

•Toevaluate overall success rate and complications ( if any ) associated with theuse of chitosan and sodium hypochlorite as haemostatic agents in pulpotomyprocedures for irreversible pulpitis.

•Tocompare sealing ability of MTA and Neoputty as pulpotomy medicaments and to evaluatethe clinical and radiographic outcomes of permanent teeth following pulpotomyprocedure .

CLINICAL SUCCESS CRITERIA

Postoperative pain incidence will benoted on the basis of visual analogue scale.

•Absenceof pain and discomfort except during the first week after treatment

•Normalmobility of the tooth

•Notenderness to percussion

•Normalsoft tissues around the tooth with no swelling or sinus tract

RADIOGRAPHIC SUCCESS CRITERIA

A baseline postoperative periapicalradiograph will be obtained using radiovisiographywhich will be used during comparative evaluation at 6months and 12 months .Nopathosis evident on the radiograph such as root resorption , furcal pathosis orperiapical pathosis.

Study Design

Study Type
Interventional
Allocation
Not Applicable
Masking
Participant and Outcome Assessor Blinded

Eligibility Criteria

Ages
18.00 Year(s) to 60.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • •Patient should be more than 18 years old Permanent teeth with deep carious lesion Tooth giving positive response to cold testing or ept and diagnosed as irreversible pulpitis .
  • •No signs of pulpal necrosis including swelling and sinus tract .
  • •The tooth should be restorable with normal probing depth.

Exclusion Criteria

  • •Moderate or severe marginal periodontitis Non restorable teeth , presence of sinus tract or swelling .
  • •Active systemic disease ( asa ii, iii,iv,v ) Negative response to cold test and ept .
  • •Pregnant and nursing women .
  • •Absence of bleeding from any canals.

Outcomes

Primary Outcomes

Absence of pain and discomfort except during the first week after treatment

Time Frame: 1 week , 6 months , 12 months

Normal mobility of the tooth

Time Frame: 1 week , 6 months , 12 months

Secondary Outcomes

  • No pathosis present on radiovisiography(6 months & 12 months)

Investigators

Sponsor
Government Dental College and hospital Ahmedabad
Sponsor Class
Other [GOVERNMENT DENTAL COLLEGE ]

Study Sites (1)

Loading locations...

Similar Trials