Status:
COMPLETED
Role of Propolis Endodontic Irrigant on Post-Operative Pain
Lead Sponsor:
Dow University of Health Sciences
Conditions:
Post-operative Pain
Symptomatic Irreversible Pulpitis
Eligibility:
All Genders
18-60 years
Phase:
PHASE3
Brief Summary
The goal of this clinical trial is to compare propolis and sodium hypochlorite as endodontic irrigants in patients presenting with symptomatic irreversible pulpitis. . The main question it aims to an...
Detailed Description
Sodium hypochlorite as an endodontic irrigant, poses problems of toxicity. Additionally, its unfavorable odor, taste, failure to remove the smear layer, and proteolytic effect have deleterious effects...
Eligibility Criteria
Inclusion
- ASA-I and II individuals who are between the ages of 18 and 60 years.
- Patients with mandibular and maxillary premolars who have been diagnosed with symptomatic irreversible pulpitis (with either a normal periapex or symptomatic apical periodontitis).
- Patients who score moderate to severe (4-10) on a preoperative visual analogue scale (VAS=1-10)
Exclusion
- Patients suffering from severe pain because of traumatic occlusion.
- Teeth with extensive damage, calcified canals, periapical radiolucency, root resorption, and an open apex.
- Patients with compromised medical condition (ASA-III and above)
- Patients who are unable to communicate effectively in either Urdu or English.
- Pregnant and lactating ladies
- Patients who are allergic to honey or bee pollen.
Key Trial Info
Start Date :
April 1 2023
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
August 15 2023
Estimated Enrollment :
44 Patients enrolled
Trial Details
Trial ID
NCT05974748
Start Date
April 1 2023
End Date
August 15 2023
Last Update
September 7 2023
Active Locations (1)
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1
Dow International Dental College
Karachi, Sindh, Pakistan, 75500