Ultra X: Evaluation of Post Operative Pain After Ultrasonic Activation and Manual Dynamic Agitation As Final Irrigation Protocols During Root Canal Treatment

Sponsor
Armed Forces Institute of Dentistry, Pakistan (Other)
Overall Status
Recruiting
CT.gov ID
NCT05852444
Collaborator
(none)
60
1
2
7
8.6

Study Details

Study Description

Brief Summary

The study analyzes the difference in post operative pain after root canal therapy, after using different activation protocols and devices. The subjects are divided into 2 groups and a different activation protocol is used in each group. In one group, final activation of irrigating agent during root canal therapy is done with an ultrasonic activation device, and in the other group, manual dynamic agitation is done using master gutta percha cone. The Post operative pain is then compared at 6, 12, 24, 48, and 72 hour intervals

Condition or Disease Intervention/Treatment Phase
  • Device: Passive Ultrasonic Activation
  • Device: Manual Dynamic Agitation
N/A

Detailed Description

Root canal therapy is a procedure in which inflamed pulp tissue and microorganisms are removed from root canals and pulp chamber, in order to eradicate infection and symptoms. Irrigation is a crucial step of an endodontic therapy and different methods and protocols are used to enhance the efficacy of irrigation. Ultrasonic activation of root canal irrigation agent is one of the effective methods that enhance the outcomes and success rate of endo therapies. It removes the smear layer, bacterial biofilms and debris by acoustic streaming and agitating the irrigant inside root canals. Similarly, a conventional method of agitation (manual dynamic agitation) also play an important role in endodontic therapy, particularly by improving the delivery of irrigation agent to the apex of a root canal. The later method involves agitation of irrigant with master gutta percha cone with continuous to and fro strokes manually.

In this study, the efficacy of both the different irrigation protocols will be compared and assessed based on post-operative pain, measured by Visual Analog Scale (VAS).

Study Design

Study Type:
Interventional
Anticipated Enrollment :
60 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Participants to be divided into 2 different groups randomly, and intervention protocol to be performed as per group designationParticipants to be divided into 2 different groups randomly, and intervention protocol to be performed as per group designation
Masking:
Double (Participant, Outcomes Assessor)
Masking Description:
Participants of the study and outcomes assessor would not know the details of groups, and only the investigator and care provider would be aware of that, as they cannot be blinded due to the nature of this study
Primary Purpose:
Prevention
Official Title:
Comparison of Postoperative Pain After Using Passive Ultra Sonic Activation (PUA) and Manual Dynamic Agitation (MDA) During Root Canal Treatment
Actual Study Start Date :
May 1, 2023
Anticipated Primary Completion Date :
Oct 31, 2023
Anticipated Study Completion Date :
Nov 30, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Group A

Passive Ultrasonic Activation Group: In this group, final activation during endodontic therapy shall be done using an ultrasonic activation device (Ultra X)

Device: Passive Ultrasonic Activation
Agitation of root canal irrigation solution with an ultrasonic activation device (Ultra X).

Experimental: Group B

Manual Dynamic Agitation Group: Irrigation in this group shall be done using a master gutta percha cone during root canal therapy

Device: Manual Dynamic Agitation
Agitation of root canal irrigation solution with master gutta percha cone

Outcome Measures

Primary Outcome Measures

  1. Post Operative pain assessed by VAS after endodontic therapy [1 week]

    comparative evaluation of post operative pain after using different irrigation devices, using VAS (Visual Analog Scale). It is drawn as a straight line of 10 inches and marked in numbers which show intensity of pain, from 0-10, with 0 being no pain at all to10 being the worst pain imaginable. In detail, it is a scale which shows pain intensity in ascending order and can also be used to analyze the intensity of pain experienced by the patient. 0: No pain at all 1-3: mild pain 4-6: moderate pain 7-9: severe pain 10: worst pain imaginable

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 60 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  1. Patients with unremarkable/ noncontributory medical history

  2. Healthy persons between the ages of 18 and 60 years

  3. Maxillary and mandibular molar teeth diagnosed with symptomatic irreversible pulpitis.

  4. Patients not having taken any medication for 6 hours before treatment

  5. No allergies to the drugs or dental material being used in the treatment

Exclusion Criteria:
  1. Patients who had taken analgesics on anti-inflammatory drugs within the last 12 hours

  2. Pregnant women and patients with immunocompromised health state

  3. Patients having severe malocclusion associated with traumatic occlusion

  4. Teeth with calcified canals

  5. Teeth with periapical radiolucency

  6. Teeth with root resorption

  7. Teeth previously undergone root canal treatment

Contacts and Locations

Locations

Site City State Country Postal Code
1 Armed Forces Institute of dentistry Rawalpindi Punjab Pakistan 64000

Sponsors and Collaborators

  • Armed Forces Institute of Dentistry, Pakistan

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Ahmed Abdullah, Registrar Operative Dentistry and Endodontics, Armed Forces Institute of Dentistry, Pakistan
ClinicalTrials.gov Identifier:
NCT05852444
Other Study ID Numbers:
  • Ultrasonic Activation
First Posted:
May 10, 2023
Last Update Posted:
May 10, 2023
Last Verified:
May 1, 2023
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Product Manufactured in and Exported from the U.S.:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 10, 2023