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Clinical Trials/CTRI/2025/03/083165
CTRI/2025/03/083165
Not yet recruiting
Not Applicable

Physiological and Pathological Predictive factors for the incidence of post-operative pain following Single Visit Endodontics: A Clinical Study

Dr Sumit singh1 site in 1 country198 target enrollmentStarted: April 25, 2025Last updated:

Overview

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
Dr Sumit singh
Enrollment
198
Locations
1
Primary Endpoint
identification of parameters causing pain following single visit root canal

Overview

Brief Summary

Patient reporting to opd Eligibility criteria will be checked based on exclusion and inclusion list and an informed consent

will be taken from patients included in the study and patients will be informed about the treatment procedure.

Assessment of preoperative pain predictors will be done.Case history will be taken. Any medical conditions to patient will be evaluated Pre-operative RVG will be taken.

Local anaesthetics (lidocaine hydrochloride and epinephrine 1:100 000) will be injected

Access will be prepared with an endo access bur NO 3 (Dentsply), using an air turbine handpiece and under water coolant. The affected tooth will be isolated with a rubber dam.

Working length will be determined and cleaning and shaping will be done using protaper gold rotary file system

Cleaning and shaping of the root canal till size F3 will be done (protaper gold rotary file system). Radiograph will be taken to check whether file and gutta ourcha cone is beyond or at apex.

Cleaning Will be performed with 5% NAOCL AND SALINE solution will be used as final irrigant. Apical patency will be maintained throughout shaping and cleaning procedures with a size 10 k-file, passed 1 mm beyond the working length

AH plus sealer will be placed into the canal using the master cone (having the same size as the apical file) as a carrier and obturation will be done. Post endo restoration will be done.

Post operative pain will be recorded on visual analogue scale After treatment, 6 hours after treatment, 12 hours after treatment, 24 hours after treatment, 48 hours after treatment, 72 hrs

Study Design

Study Type
Observational

Eligibility Criteria

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

Inclusion Criteria

  • Age between 18-60 years Patients who have signed the consent Symptomatic/asymptomatic irreversible pulpitis Symptomatic/asymptomatic apical periodontitis Periapical pathology.

Exclusion Criteria

  • Pregnancy Failure to obtain authorization from patients or the presence of accidents or complications during treatment Obliterated canals Periodontally compromised teeth Inability to achieve apical patency in any canal Swelling Endodontic emergency Patient with Temporomandibular joint pain Patient having premedication (analgesia and antibiotic) Non-surgical retreatment cases.

Outcomes

Primary Outcomes

identification of parameters causing pain following single visit root canal

Time Frame: 6hr, 12hr,24hr,48hr,72hrs

Secondary Outcomes

  • identification of parameters causing pain following single visit root canal(6hr, 12hr,24hr,48hr,72hrs)

Investigators

Sponsor
Dr Sumit singh
Sponsor Class
Private medical college
Responsible Party
Principal Investigator
Principal Investigator

Dr Sumit singh

Army college of dental sciences

Study Sites (1)

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