Status:
ACTIVE_NOT_RECRUITING
Measure Postoperative Pain and Bacterial Reduction After Different Final Irrigation Protocols.
Lead Sponsor:
Future University in Egypt
Conditions:
Symptomatic Irreversible Pulpitis (SIP)
Eligibility:
All Genders
18-40 years
Phase:
NA
Brief Summary
The primary objective of root canal treatment is to clean, disinfect, and hermetically seal the root canal system to prevent bacterial penetration; however, postoperative pain is frequently encountere...
Eligibility Criteria
Inclusion
- Patients with age range between 18 to 40.
- No sex predilection.
- Patients with symptomatic irreversible pulpitis.
- Patients able to sign informed consent.
- Restorable teeth
- Positive patient's acceptance for participating in the study.
- Type III distal and mesial canal of first mandibular molar.
- Mild to moderate (5-20) ° curvature according to Schneider
Exclusion
- Pregnant females
- Medically compromised patients.
- Patients having analgesics before the treatment
- If antibiotic have been administrated during the past two weeks preoperatively.
- Patients having bruxism or clenching
- Patients having sever malocclusion associated with traumatic occlusion.
- Teeth that have:
- Peri-apical periodontitis Root resorption Pain on percussion Pulp stones or calcifications Previous endodontic treatment.
- Non-patent canals
Key Trial Info
Start Date :
July 1 2025
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
March 1 2026
Estimated Enrollment :
60 Patients enrolled
Trial Details
Trial ID
NCT07191990
Start Date
July 1 2025
End Date
March 1 2026
Last Update
September 25 2025
Active Locations (1)
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1
Future University in Egypt
Cairo, New Cairo, Egypt, 11835