Actively Recruiting
Effectiveness of Intracanal Cryotherapy on Post Operative Pain After Root Canal Therapy in Patients with Symptomatic Apical Periodontitis
Led by Armed Forces Institute of Dentistry, Pakistan · Updated on 2025-01-21
60
Participants Needed
1
Research Sites
26 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are conducting a randomized, prospective controlled trial to evaluate how intracanal cryotherapy affects pain levels after root canal treatment in patients with symptomatic apical periodontitis. The study targets adults aged 20 to 40 years who have symptomatic irreversible pulpitis with symptomatic apical periodontitis and a pain score below 8 on a visual scale from 0 to 10. This phase 2 trial aims to assess pain one week after the procedure. Participants receive local anesthesia and a rubber dam is applied before the root canal treatment. The procedure includes accessing the tooth cavity, determining working length using a file and radiograph, cleaning and shaping the canal with manual and motorized tools using sodium hypochlorite and EDTA, followed by final irrigation. Patients are divided into two groups: one receives room temperature saline irrigation, and the other receives cold saline irrigation at 2.5°C, both delivered for five minutes using a fine needle. The canals are then dried and filled with gutta percha and zinc oxide eugenol sealer, and the tooth is restored with composite or glass ionomer cement. During the study, patients record their pre-treatment pain and are instructed to monitor post-operative pain. Diagnostic assessments include medical history, clinical and radiographic exams recorded for each patient. Researchers measure post-operative pain one week after treatment. The total duration of involvement is mainly focused on this immediate treatment and follow-up period to assess pain relief. Safety considerations include excluding patients with allergies to local anesthesia or recent use of analgesics or antibiotics.
CONDITIONS
Official Title
Effectiveness of Cryotherapy on Endodontic Pain
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients with symptomatic irreversible pulpitis and symptomatic apical periodontitis
- Maxillary or mandibular single rooted teeth
- Systemically healthy patients
- Patients having pain score < 8
- Aged between 20 and 40 years
You will not qualify if you...
- Patients on preoperative analgesics or antibiotics within past 12 hours
- Teeth with calcified canals and previously treated teeth
- Tooth with immature apices or resorption
- Patients allergic to local anesthesia
- Pregnant or lactating mothers
- Patients who are immunocompromised
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Armed Forces Institute of Dentistry
Rawalpindi, Punjab Province, Pakistan, 46000
Actively Recruiting
Research Team
H
Hira Amjad, BDS
K
Kanza Zafar, BDS
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
Frequently Asked Questions
Have more questions? Get in touch with our team for quick support
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here