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A clinical trial to study the efficacy of two rotary file systems ,Protaper Gold and XP EndoShaper in patients with symptomatic irreversible pulpitis.

Assessment of endodontic therapy with xp-endoshaper and protaper gold -a randomized clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/07/035179
Enrollment
50
Registered
2021-07-27
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: K040- Pulpitis

Interventions

Intervention1: xp endoshaper: anatomical rotary instrument, these are recently introduced rotary endodontic files which prepare the mechanical preperation of root canal according to its anatomy.These

Sponsors

Dr y sushmita
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.patients with symptomatic irreversible pulpitis with apical periodontitis 2. Patients of age group between 18-50 years. 3.Patients who will show prolonged response even after the removal of stimulus. 4.Patients will be included in the study after evaluation of electric pulp test response 5.Patient who has the ability to understand OHIP-14 and pain questionnaires will be provided informed consent for endodontic treatment

Exclusion criteria

Exclusion criteria: 1.Patients with immature teeth, sinus tract, periapical abscess or facial cellulitis. 2.Patients with generalised attrition. 3.Patients with Re -RCT will be excluded. 4.Patient with known allergies, or any contra-indication to opioid or non-opioid analgesics including aspirin or NSAIDs. 5.Patients with known allergy to local anaesthesia, sodium hypochlorite and chlorhexidine. 6.Presence of systemic diseases like cardiovascular disease, renal disease, bleeding disorders or any anti-coagulant use with in last month. 7.Pregnant and lactating mothers. 8.Patients under pain medication for dental or any other illness within 24 hours. 9.Patients who are unable or unwilling to complete the OHIP-14 and pain questionnaires. 10.Patients who are unwilling to sign consent for endodontic treatment

Design outcomes

Primary

MeasureTime frame
a) Time taken for cleaning and shaping with XP Endo Shaper and Pro Taper Gold b) To evaluate the Pre and Post peri cervical dentin when the RCT is performed with XP Endo Shaper and Pro Taper Gold c) Pain evaluation using VAS scale Timepoint: a)Pain evaluation using VAS scale at 12 , 24 , 48 and 72 hrs.

Secondary

MeasureTime frame
To evaluate the QOL (Quality Of Life) in patients undergoing RCT with XP Endo Shaper and Pro Taper GoldTimepoint: after 72 hrs

Countries

India

Contacts

Public ContactDr a lavanya

Narayana Dental College And Hospital

chinnisk@yahoo.com9966313666

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026