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Clinical Trials/ISRCTN14290358
ISRCTN14290358
Completed
Not Applicable

Assessment of the procedure duration and efficacy of pulpotomy and partial pulpectomy in comparison with total pulpectomy for patients with symptomatic irreversible pulpitis: a randomized clinical trial

Baskent University0 sites66 target enrollmentJune 8, 2017
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ConditionsSymptomatic irreversible pulpitisOral Health

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Symptomatic irreversible pulpitis
Sponsor
Baskent University
Enrollment
66
Status
Completed
Last Updated
8 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

2017 results in https://www.ncbi.nlm.nih.gov/pubmed/28857203

Registry
who.int
Start Date
June 8, 2017
End Date
April 4, 2017
Last Updated
8 years ago
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • •1\. Aged between 18 and 60 years
  • •2\. Male or female
  • •2\. Acute dental pain in posterior maxillary or mandibular molar teeth
  • •4\. Diagnosed with symptomatic irreversible pulpitis with or without symptomatic apical periodontitis

Exclusion Criteria

  • •1\. History of American Society of Anesthesiologists (1963\) III\-VI status
  • •2\. Pregnancy or nursing
  • •3\. Mental disability
  • •4\. History of allergy to nonsteroidal anti\-inflammatory drugs, and analgesic treatment during the 12 hours prior to presentation
  • •5\. If the subject tooth has moderate or severe marginal periodontitis, horizontal or vertical fractures, internal or external root resorption, root canal calcification, or a nonrestorable crown defect
  • •6\. If an opposing and/or neighbouring tooth has defective restorations, deep caries, moderate or severe marginal periodontitis, wear, or history of recent tooth preparation.

Outcomes

Primary Outcomes

Not specified

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