Comparison of Post-operative Pain After Different Root Canal Irrigant Activation Methods

ConditionsIrriversible Pulpitis Irrigation Activation, Patient

Trial statusNot yet recruiting

Trial phaseNot applicable

Trial typeInterventional

Biological sexAll

Age20-50

SponsorRANA AHMAD

About this trial

root canal irrigation protocol

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

• Patients in good health with no systemic disease (ASA Class I or II)

Age range is between 20 to 50 years.

Patients diagnosed with symptomatic irreversible pulpitis in maxillary incisor teeth.

Patients who can understand VAS.

Disqualifiers

• History of systemic disorder.

Pregnant / lactating females (As per medical record/verbally)

Patients who had taken preoperative drugs as anti-inflammatory analgesic or antibiotics.

Patients with swelling or acute peri-apical abscess.

Trial design

Design model

Parallel

Treatments tested in this trial

passive ultrasonic activation
Procedure/Surgery
passive ultrasonic irrigant activation will be performed by using a stainless steel ultrasonic Irrisafe file of size 20 (IRRI S 21/25; VDW, Germany) mounted on ultrasonic unit (Woodpecker Ultrasonic Scaler UDS-J). The file will be kept 2 mm short of working length loosely without binding to the canal. 2.5% NaOCl will be activated for 30 seconds by using a power setting of five
sonic activation
Procedure/Surgery
root canals will be filled with 2.5% sodium hypochlorite and medium size tip (red, 25/04) of EndoAcivator (YAHOPE A3, China) will be used keeping it 2 mm short of working length. The activation of irrigant will be done in 2-3 mm vertical strokes for 30 seconds in between each instrumentation

Treatment groups

72 Participants

are divided into 2 treatment groups

Group A: Passive ultrasonic activationActive comparator 1 intervention

Group B: Sonic activationActive comparator 1 intervention

Trial outcomes

Primary outcomes

pain score on visual analogue scale

After complete root canal irrigation and preparation, canals will be dried and a temporary dressing of Cavit will be placed. Patients will be reappointed for obturation. VAS scale ranging from 0-10 will be given to patient and will be demonstrated on how to record their pain and which will be recorded by the patient after 24 hours and 48 hours by marking on a chart ranging from 0-10 with 0 = no pain, 1-3 = mild pain, 4-6 = moderate pain 7-10 = severe pain. On 5th day of follow-up, obturation will be done using single cone obturation method

Time frame

48 hours

Locations

This trial has no locations.

Sponsors and contacts

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

RANA AHMAD

Lead sponsor

Shaheed Zulfiqar Ali Bhutto Medical University

Sponsor institution

Source ClinicalTrials.gov

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