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Comparison Of The Incidence Of Postoperative Pain Using Different Single File Systems: A Prospective, Randomized Clinical Trial

Completed
Conditions
this is a randomized clinical trial done on healthy human volunteers with irreversible pulpitis in mandibular molar teeth
Registration Number
CTRI/2019/12/022402
Lead Sponsor
Dr Kriti Kapoor
Brief Summary

This is a Prospective Randomized Clinical trial to evaluate postoperative pain after root canal treatment using three different single file systems.Other criterias assessed were treatment time and systemic analgesic intake at 24 hrs, 48 hrs, 72 hrs and 7 days.  Single visit root canal treatment is done to assess pain level after root canal treatment, also analgesic intake and total treatment time.   All subjects will be asked to mark pain on Heft Parkers Visual Analog Scale to analyse the level of pain. Data will be subjected to statistical analysis.

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
All
Target Recruitment
150
Inclusion Criteria
  • 1.Mandibular molars of patients aged between 18 to 40 years with no systemic disease.
  • 2.No history of trauma to the involved tooth.
  • 3.No periapical radiolucency related to the involved tooth.
  • 4.No parafunctional habit.
  • 5.No pus or inflammatory exudate draining through the canal or sinus tract.
  • 6.No tenderness on percussion in the involved tooth.
  • 7.Positive response on cold testing and electric pulp testing.
Exclusion Criteria
  • 1.Patients with non-vital teeth.
  • 2.Presence of sinus tracts or draining pus.
  • 3.Cases of apical periodontitis.
  • 4.Radiographic evidence of a periapical lesion.
  • 5.Endodontic Retreatment cases.
  • 6.Root resorption cases.
  • 7.Immature or open apex cases 8.Root canal in which patency of apical foramen could not be established.
  • 9.Patients whose teeth had issues precluding single visit treatment.
  • 10.Teeth with anatomic variations and difficult root anatomy (canal curvatures >25 degree radiographic evidence of calcification.
  • 11.Patients using some type of medication preoperatively such as analgesics or steroidal anti-inflammatory drugs.
  • 12.Patients with any uncontrolled systemic diseases.
  • 13.Patients with allergies to sodium hypochlorite.
  • 14.Medically compromised patients.
  • 15.Missing antagonist tooth.
  • 16.Pregnant women.
  • 17.Teeth with wide canals.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To compare postoperative pain after root canal treatment using different single file systems .Pain assessment of the patient after 24 hrs,48 hrs, 72 hrs and 7 days
Secondary Outcome Measures
NameTimeMethod
Time taken for the treatment in every patient;Systemic analgesic intake of patient if any

Trial Locations

Locations (1)

SGT Dental College, Hospital & Research Institute

🇮🇳

Gurgaon, HARYANA, India

SGT Dental College, Hospital & Research Institute
🇮🇳Gurgaon, HARYANA, India
Dr Kriti Kapoor
Principal investigator
08076872106
kriti2060@gmail.com

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