Clinical Trials Directory

Trials / Completed

CompletedNCT07233577

The Effect of Dexamethasone in Full Pulpotomy on Postoperative Pain in Permanent Molars

The Effect of Dexamethasone in Full Pulpotomy on Postoperative Pain in Permanent Molars With Symptomatic Irreversible Pulpitis: A Randomized Clinical Study

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
72 (actual)
Sponsor
Cukurova University · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

The goal of this clinical trial is to evaluate the effects of cryotherapy and dexamethasone on the intensity of postoperative pain in full pulpotomy procedures in permanent molars with symptomatic irreversible pulpitis. The main questions it aims to answer are: * Does controlled irrigation with cold saline during full pulpotomy reduce the severity of postoperative pain? * Does controlled irrigation with dexamethasone during full pulpotomy reduce the severity of postoperative pain? In the cryotherapy group, unlike the control and dexamethasone groups, the pulp chamber was irrigated with 2°C saline solution during the final irrigation step. In the dexamethasone group, unlike the control and cryotherapy groups, the pulp chamber was irrigated with 2 mL dexamethasone solution during the final irrigation step.

Conditions

Interventions

TypeNameDescription
OTHERCryotherapyIn the cryotherapy group, the pulp chamber was irrigated with 5 mL of sterile saline solution pre-cooled to 2.5°C during full pulpotomy.
DRUGDexametasoneIn the dexamethasone group, the pulp chamber was irrigated with 2 mL of dexamethasone sodium phosphate solution (4 mg/mL) during full pulpotomy.

Timeline

Start date
2024-12-18
Primary completion
2025-05-05
Completion
2025-06-16
First posted
2025-11-18
Last updated
2025-11-24

Locations

1 site across 1 country: Turkey (Türkiye)

Source: ClinicalTrials.gov record NCT07233577. Inclusion in this directory is not an endorsement.