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RECRUITING
NCT07459049
PHASE4

"Effect of Ibuprofen on Acute Inflammatory Response After One-Stage Periodontal Therapy"

Sponsor: University of Baghdad

View on ClinicalTrials.gov

Summary

The goal of this ( Clinical Trial ) is to evaluate the efficacy of Ibuprofen in reducing acute inflammatory response (hs-CRP, ProCT, IL-6) after one hour and one week following one stage non surgical periodontal therapy. The main question it aims to answer is: "Does Ibuprofen effectively reduce the acute inflammatory response ( hs-CRP, ProCT, IL-6) following one-stage non-surgical periodontal therapy?"

Official title: Efficacy Of Ibuprofen In Reducing Acute Inflammatory Response Following One Stage Non- Surgical Periodontal Therapy (A Randomized Clinical Trial )

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

30

Start Date

2025-12-01

Completion Date

2026-08

Last Updated

2026-03-09

Healthy Volunteers

No

Conditions

Interventions

PROCEDURE

Non surgical root surface debridement in one stage without receiving Ibuprofen

Control group: After one week from baseline visit which include supragingival debridement by using ultrasonic device . sites will receive root surface debridement (RSD) using area specific (Gracey) curettes (Medesy, Italy). Without receiving Ibuprofen.

DRUG

Non surgical root surface debridement in one stage with receiving Ibuprofen

Test group: After one week from baseline visit which include supragingival debridement by using ultrasonic device . Test group will receive first dose of Ibuprofen (400 mg) administer one hour before root surface debridement and the subsequent doses will be taken 3 times daily for a duration of 3 days after RSD.

Locations (1)

College of Dentistry, University of Baghdad

Baghdad, Iraq