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Clinical Trials in Italy / NCT07712432
Recruiting Observational

Insomnia and Post-Dental Surgery Pain: A Prospective Study

NCT07712432 · tracked via the Priya Life Science Italy tracker
Phase
Observational
Started
2026-09-01
Last updated
2026-09-03

Condition(s) studied

DentalDental ExtractionInsomnia

Study summary

The purpose of this prospective observational study is to evaluate the relationship between preoperative sleep disturbances-specifically insomnia-and postoperative pain intensity following oral surgical procedures. Recent scientific literature highlights a bidirectional relationship between sleep disorders and pain in dentistry, suggesting that disturbed sleep may actively exacerbate subsequent pain perception. Although postoperative pain, swelling, and masticatory difficulties are common after dental extractions, clinical data investigating the direct impact of preoperative sleep quality on these surgical outcomes remain scarce. This study will enroll adult patients undergoing routine dental extractions and allocate them into two cohorts based on their baseline sleep quality: patients without preoperative sleep disturbances and patients with preoperative sleep disturbances. Pain levels and sleep parameters will be assessed using validated questionnaires before the surgery and at a 7-day follow-up. The primary objective is to determine whether the presence of preoperative insomnia leads to a significant increase in perceived postoperative surgical pain.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Age over or egual 18 years. * Need for odontoiatric surgical intervention (dental extractions). * Willingness to participate in the study by completing the proposed questionnaires. * Good understanding of the Italian language. * Ability to understand and sign the informed consent form. Exclusion Criteria: * Pharmacological therapy interfering with sleep or pain at the time of recruitment. * Acute pain or ongoing infections at the time of recruitment. * Relevant comorbidities. * Pregnancy. * Impossibility to complete the follow-up.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Clinica Odontoiatrica; Fondazione Universitaria Policlinico A.Gemelli IRCCS Roma Italy Recruiting

More Fondazione Policlinico Universitario Agostino Gemelli IRCCS trials in Italy

Other trials for the same condition

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 NCT07712432 on ClinicalTrials.gov ↗ ← All trials in Italy