← Back to Clinical Trials
Recruiting NCT07310212

Evaluation of Postoperative Pain and Success Rate Between Lateral Condensation and Warm Vertical Obturation Techniques

◆ AI Clinical Summary
Plain-language summary for patients

Trial Parameters

Condition Necrotic Pulp
Sponsor University of Jordan
Study Type INTERVENTIONAL
Phase N/A
Enrollment 80
Sex ALL
Min Age 18 Years
Max Age N/A
Start Date 2024-10-17
Completion 2026-06-01
Interventions
Warm Vertical Condensation (WVO)Cold Lateral Condensation (CLC)

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

Brief Summary

Brief Summary Postoperative pain is a common complication following root canal treatment, particularly in necrotic teeth with asymptomatic apical periodontitis. Although obturation technique has been suggested as a contributing factor to postoperative discomfort, direct clinical comparisons between commonly used methods remain limited. Cold lateral condensation has traditionally been considered the standard obturation technique, while warm vertical obturation systems such as Obtura II have gained popularity due to their potential for improved adaptation of gutta-percha. This randomized controlled clinical trial aims to compare postoperative pain experience and treatment outcomes following cold lateral condensation and warm vertical obturation in single-rooted necrotic teeth. Postoperative pain will be assessed during the early healing period, along with patient-reported outcomes and short-term clinical and radiographic healing. The results of this study are expected to provide clinically relevant evidence to support evidence-based obturation technique selection and improve patient comfort in endodontic practice.

Eligibility Criteria

Inclusion Criteria: * Adults aged 18 years or older. * Patients requiring endodontic treatment for single-rooted necrotic teeth. * Radiographic and clinical diagnosis of asymptomatic apical periodontitis. * Ability to understand the study and provide written informed consent. Exclusion Criteria: * Teeth diagnosed with symptomatic apical periodontitis. * Pregnant or lactating women. * Patients with systemic diseases affecting pain perception (e.g., uncontrolled diabetes, chronic pain conditions). * Teeth that have been previously endodontically treated. * Patients taking medications that may influence pain perception (e.g., chronic analgesic or anti-inflammatory drug use). * Periodontally compromised teeth with significant bone loss or mobility.

Related Trials

ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology
}