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Clinical Trials/CTRI/2017/02/007774
CTRI/2017/02/007774
Completed
Phase 4

EVALUATION OF POST OPERATIVE PAIN IN SINGLE VISIT ROOT CANAL TREATMENT WITH PROTAPER NEXT AND M TWO ROTARY SYSTEMS IN ASYMPTOMATIC IRREVERSIBLE PULPITIS OF MULTIROOTED TEETH-A RANDOMIZED CLINICAL TRIAL. - EPSRT

arayana dental college and hospital0 sites40 target enrollmentTBD
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Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Not specified
Sponsor
arayana dental college and hospital
Enrollment
40
Status
Completed
Last Updated
4 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
4 years ago
Study Type
Interventional

Investigators

Sponsor
arayana dental college and hospital

Eligibility Criteria

Inclusion Criteria

  • •1\.Multi rooted teeth with asymptomatic irreversible pulpitis with normal periapical radiographic appearance and periapical radiolucency less than 2mm will be scheduled for initial endodontic treatment.
  • •2\.Patients of age group between 18\-50
  • •3\.Subjects who will show prolonged response even after the removal of the stimulus.
  • •Patient who has the ability to understand the use of pain scales will be provided informed consent for endodontic treatment.

Exclusion Criteria

  • •1\.Patients with sinus tract, periapical abscess or facial cellulitis.
  • •2\.Patient with known allergies, or any contraindication to opioid or non\-opioid analgesics including aspirin or NSAIDs.
  • •Patients with known allergy to local anaesthesia, sodium hypochlorite and chlorhexidine. Presence of systemic diseases like cardiovascular disease, renal disease, and any bleeding disorders or anti coagulant use with in last month.
  • •3\.Pregnants and lactating mothers.
  • •4\.Patients under pain medication for any other illness.
  • •5\. Patients who are unable or unwilling to complete the pain questionnaires;
  • •6\. Patients who are unwilling to sign consent for endodontic treatment

Outcomes

Primary Outcomes

Not specified

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