Comparing Post Operative Pain With and Without Apical Patency Technique in Asymptomatic Irreversible Pulpitis Teeth

ConditionAsymptomatic Irreversible Pulpitis

Trial statusNot yet recruiting

Trial phaseNot applicable

Trial typeInterventional

Biological sexAll

Age20-50

SponsorBolan Medical Complex Hospital Quetta Pakistan

About this trial

Primary Outcome - Measure Presence of postoperative pain Primary Outcome - Time Frame 24 hours post-treatment Primary Outcome - Description Postoperative pain assessed using the Numerical Rating Scale (NRS), categorized as present (NRS ≥1) or absent (NRS = 0)

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

None

Disqualifiers

None

Trial design

Design model

Parallel

Treatments tested in this trial

Apical Patency Technique
Procedure/Surgery
After each rotary instrument, a pre-curved #10 K-file was passively passed 0.5 mm beyond the working length. No filing motion was performed.
Non-Patency Technique
Procedure/Surgery
No instrument was intentionally passed beyond the working length. Recapitulation was performed only to the working length.

Treatment groups

150 Participants

are divided into 2 treatment groups

Group A: Apical Patency GroupExperimental treatment 1 intervention

Group B: Non-Patency GroupActive comparator 1 intervention

Trial outcomes

Primary outcomes

Primary Outcome - Measure Presence of postoperative pain

Postoperative pain assessed using the Numerical Rating Scale (NRS), categorized as present (NRS ≥1) or absent (NRS = 0)

Time frame

24 hours post-treatment

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Bolan Medical Complex Hospital Quetta Pakistan

Lead sponsor

Source ClinicalTrials.gov

This trial is not recruiting at the moment. You can still explore other options: