Comparison Between Two Instrumentation Techniques on Postoperative Pain and Level of Neuropeptides
Condition(s) studied
Investigational drug(s) / intervention(s)
Manual-less: Canals preparation with rotary dota files escaping scouting and glide path step
Conventional technique: Canal preparation with rotary drill files, with prior scouting and glide path with hand files.
Study summary
General aim: assessment of post operative pain and time of preparation with the execution of manual-less technique and conventional technique.
Specific aim: correlation between post operative pain and release of Substance P and Calcitonin gene-related peptide.
Eligibility
Primary outcome measure(s)
- Change in post operative pain — 6 hours,12 hours,24 hours,48 hours,72 hours
Numeric rating scale ranges from zero to 10. zero means no pain and 10 means severe pain.
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Alexandria Faculty of Dentistry | Alexandria | Egypt | Recruiting |
More Alexandria University trials in Egypt
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT07357233 on ClinicalTrials.gov ↗ ← All trials in Egypt