Sapienza University of Rome
Rome, 00161, Italy
NCT Number: NCT06738342
The primary objective of the study is the evaluation of efficacy of a mouthwash cointaining Chlorexidine (CHX) 0.09% + HA + Citrox (test group) on the quality of wound healing and the presence plaque formation and gingival inflammation in the post-surgical phase. Futhermore stains, discolorations and adverse effects will be eventually recorded. Control group will be represented by the use of a CHX 0.12% mouthwash.
Trial opening soon.
Get Notified18 year–65 year
All sexes
Interventional
Not applicable
Rome, 00161, Italy
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
The patient will use the assigned mouthwash starting 24 hours after the surgical procedures and continuing twice a day for 14 days.
The patient will use the assigned mouthwash starting 24 hours after the surgical procedures and continuing twice a day for 14 days.
Time frame: 1, 3, 7 an 14 days
Presence of absence will be recorded (1 or 0).
Time frame: 24 hours post surgery, 3, 7 and 45 days post surgery
The score comprises three parameters (Clinical signs of re-epithelialization, hemostasis and inflammation) and ranges from 0 (worst healing) to 10 (best healing)
Time frame: 1,3,7 and 14 days post surgery
Time frame: 1,3,7 and 14 days post surgery
Time frame: 1,3,7 and 14 days post surgery
Presence of stains or discolorations of teeth and mucosae
Time frame: 1,3,7 and 14 days post surgery
Disgeusia, mouth ulcers
Trial opening soon.
Get NotifiedUniversity of Roma La Sapienza
Other
Clinical Efficacy of a Chlorhexidine-based Mouth-rinse Containing Citrus Aurantium Amara in Patients Undergoing Periodontal Surgery: a Triple-blind, Parallel-arm, Randomized Controlled Trial
Acronym: CUR_01
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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