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Recruiting Not applicable

Comparison Between Two Instrumentation Techniques on Postoperative Pain and Level of Neuropeptides

NCT07357233 · tracked via the Priya Life Science Egypt tracker
Phase
Not applicable
Started
2025-09-01
Last updated
2026-01-21

Condition(s) studied

Post Operative Pain

Investigational drug(s) / intervention(s)

Manual-lessConventional technique

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

Sex
ALL
Min age
18 Years
Max age
50 Years
Healthy volunteers
Accepted
Inclusion Criteria: 1. Patients with symptomatic irreversible pulpitis and apical periodontitis in mandibular molars with closed apex.(17) 2. Healthy males and females (Category: American Society of Anesthesiologists class I). 3. Age of patients range from 18 to 50 years old. 4. Those who could understand the use of the numeric rating scale (NRS) for pain. 5. In cases where radiographs show no root resorption or abnormal anatomy. 6. Patients with good oral hygiene and free from periodontal diseases. Exclusion Criteria: 1. Allergy to anesthetics. 2. Pregnancy 3. Unrestorable teeth. 4. Patient on analgesics. 5. Prescence of root resorption or abnormal anatomy.

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)

FacilityCityRegionStatus
Alexandria Faculty of Dentistry Alexandria Egypt Recruiting
Official registry record

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