CLINICAL TRIALS PROFILE FOR RID MOUSSE
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All Clinical Trials for Rid Mousse
| Trial ID | Title | Status | Sponsor | Phase | Start Date | Summary |
|---|---|---|---|---|---|---|
| NCT01851681 ↗ | Comparison Between Two Different Antibiotic Regimens for the Placement of Dental Implants | Completed | Université de Montréal | Phase 1 | 2014-07-01 | In order to prevent infections and complications, it has been initially established with the dental implant placement protocol that pre- and post-operative antibiotics should be prescribed to the patient receiving dental implants. There have been many antibiotic regimens used in the attempt to minimize the risks of infections and consequently, increasing the survival rate of dental implants placement procedures. However, issues about bacterial resistance have been raised recently concerning the extensive use of antibiotics. The primary objective of this study is to find out whether giving antibiotics before or after implant placement would significantly influence crestal bone loss around dental implants. One study group will receive one dosage of antibiotics before implant placement followed by post-operative intake of antibiotics for 7 days. Another group will receive the antibiotics in one single preoperative dose followed by an identical placebo for 7 days. Questionnaires for pain and interference with daily activities assessment to be filled for the first postoperative week will be distributed to participants. Signs of postoperative morbidity will be recorded at 1 and 3 weeks following the surgery, and both clinical and radiographic data will be collected at 4 months postoperative to assess the implants status. A radiographic follow-up will be done 1 year after the surgery. Peri-implant crevicular fluid levels of 3 known immunological markers for bone loss (MMP-8, sRANKL and OPG) will be measured at 1-, 3- and 16-weeks follow-ups. The findings from this study might allow clinicians to establish the ideal antibiotic regimen with minimal risk exposure to bacterial resistance. |
| NCT03355846 ↗ | Pain and Bleeding in Subjects With Acute Anal Fissure: Comparative Evaluation of Three Treatments | Completed | University of Roma La Sapienza | Phase 4 | 2018-05-01 | Starting from the observation that acute anal fissure (AAF) in 6-8 weeks can heal spontaneously and that some of the commonly used commercial products in clinical practice would seem to be useful, the rationale of the comparative study is to try to identify, in compliance with the protocol of Helsinki (2013), the most effective short-term treatment for the disappearance of pain in defecation and cessation of bleeding, shortening the duration of the healing process and favoring the patient's rapid return to his / her activity, respect for patient safety. |
| NCT03391180 ↗ | The Effect of ICON Treatment on WPL With Patients After Fixed Orthodontic Appliances | Unknown status | Riyadh Colleges of Dentistry and Pharmacy | N/A | 2018-02-01 | The aim of this study is to determine the effect of ICON on White spot lesions compared to CPP-ACPF plus. |
| >Trial ID | >Title | >Status | >Sponsor | >Phase | >Start Date | >Summary |
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