Isala Hospital
Zwolle, Overijssel, 8025AB, Netherlands
NCT Number: NCT06880952
This study aimed to assess the impact of postoperative chlorhexidine use on pain management following mandibular third molar removal
In this prospective, randomized controlled trial,130 patients who underwent mandibular third molar surgical removal were divided into two groups: one group used chlorhexidine for postoperative rinsing and the other did not rinse. Pain levels, measured using the Numeric Rating Scale (NRS), were recorded daily for the first seven days post-surgery. Paired-samples t-tests were utilized for data analysis.
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Notify Me18 year and older
All sexes
Interventional
Not applicable
Zwolle, Overijssel, 8025AB, Netherlands
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
In the rinsing group, the patients received a bottle of 0,2% chlorhexidine
Time frame: 7 days after the inclusion pain was measured on a numerical rating scale
The primary endpoint is the difference in the postoperative pain measured on a numerical rating scale (NRS) evaluated at seven days
Time frame: 7 days after the treatment the patient was seen at the outpatient clinic for clinical assessment. At this moment the number of patients with alveolitis, foodimpaction and bleeding was scored.
As secondary outcome measures alveolitis, foodimpaction, bleeding or infection
Isala
Other
Effect of Post-operative Chlorhexidine on Postoperative Pain and Complications After Surgical Removal of Mandibular Third Molars: a Randomized Controlled Trial
Acronym: RITOR
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