Clinical Trials Logo

Clinical Trial Summary

Objective: This randomized, controlled clinical study aimed to evaluate the performance of one universal adhesive applied with etch-and-rinse or self-etch strategy and one etch-and-rinse adhesive on fissure sealant retention over 24 months. Methodology: 144 sealants were placed on the permanent premolars and molars of 13 subjects. Teeth were divided into three groups SB2(control): Adper Single Bond 2, SBU-ER: Single Bond Universal/etch-and-rinse, SBU-SE: Single Bond Universal/self-etch. After the adhesive application, Fissurit FX was applied and light-cured. Clinical evaluations were done at baseline and at 1 week, 6-, 12-, 18- and 24-month recalls. Visual examination was performed on every visit for evaluation of the sealants. Evaluating criteria were: 1= completely retained; 2= partial loss; 3= total loss. The Pearson Chi-square test was used for each evaluation period.


Clinical Trial Description

Thirteen patients with a mean age of 20.5 (range 19-22) were selected among the patients seeking routine dental care from Conservative Dentistry Department who met the inclusion criteria. Inclusion criteria were: good oral hygiene and and the absence of caries, previously placed restorations, bruxism and an allergy to the materials tested. Bitewing radiographs were taken. Pellicle and any remaining plaque on the fissures were removed by using slurry of pumice with a slow-speed handpiece. All restorative procedures were performed by the same operator. The teeth were assigned for different group by using a table of random numbers. Group 1 (SB2): Etched with 35% phosphoric acid gel for 30 s, rinsed and dried. Adper Single Bond 2 (3M ESPE St. Paul MN. USA) applied and light cured for 10s with a LED device (Demi Plus; Kerr, Switzerland) Group 2 (SBU-ER) : Etched with 35% phosphoric acid gel for 30s, rinsed and dried. Single Bond Universal Adhesive (3M ESPE St. Paul MN.USA) applied, gently air thinned for 5 s and light cured for 10s with a LED device Group 3 (SBU-SE): Single Bond Universal Adhesive (3M ESPE St. Paul MN.USA) applied for 20 s with vigorous agitation, gently air thinned for 5 s and light cured for 10 s with a LED device A nanofilled fissure sealant, Fissurit FX (Voco,Cuxhaven,Germany) was applied to the fissures and air entrapment was prevented by carefull spreading with a dental probe. The sealant material was light-cured for 20 seconds with LED. The occlusion was checked with articulating paper. Fine-grit diamond burs (Diatech, Swiss Dental, Switzerland) and rubber cups (Edenta AG, AU SG, Switzerland). were used for finishing and polishing. Each restoration was evaluated at baseline,1week after treatment and 6, 12, 18 and 24 months. Evaluation of restorations was carried out by two calibrated examiners who were unaware of group allocation and who were not involved with the treatment procedures, by the help of a mirror, blunt explorer and air stream. Caries formation was evaluated as present or absent and the sealants were evaluated according to the following criteria: 1= Completely retained 2= Partial loss 3= Total loss. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04837469
Study type Interventional
Source Ondokuz Mayis University
Contact
Status Completed
Phase N/A
Start date January 1, 2014
Completion date March 1, 2016

See also
  Status Clinical Trial Phase
Recruiting NCT05265559 - Influence of Operator Factors on Succes and Survival of Indirect Restorations
Not yet recruiting NCT04641923 - The Efficacy of a Topical Anti-adhesive Film for Decreasing Perihepatic Adhesions in Repeat Hepatic Surgery N/A
Completed NCT03443583 - Immediate and Delayed Dentin Sealing Effect on Partial Crowns N/A
Completed NCT03660787 - Efficacy and Dose Ranging Study of Seroguard Phase 2
Completed NCT03640559 - Safety and Tolerability of Seroguard Use Phase 1
Active, not recruiting NCT04271150 - Efficiency of Different Modes of Universal Adhesive N/A
Recruiting NCT05580471 - A Randomized Control Study of Anti-Adhesion Agent After Colorectal Surgery N/A
Active, not recruiting NCT02434601 - Dentin Treatments for Restorations of Cervical Lesions Non-Carious Phase 2/Phase 3
Recruiting NCT05811585 - PMCF Study for ADEPT® in LaparoscopicGynecologic Surgery
Completed NCT05036525 - Evaluation of the Efficacy and Safety of a Hyaluronic Acid Gel in Adhesion Prevention After Open Thyroidectomy. N/A
Not yet recruiting NCT04475367 - Evaluation of the Effect of an APP in Improving Treatment Adherence in Hypertensive Patients in Hypertension Ambulatory N/A
Completed NCT03293186 - Anti-adhesive Effect and Safety of "Thermo-sensitive Adhesion Barrier (MEDICLORE)" Phase 4
Completed NCT04023383 - New Cross Linked Hyaluronan Gel After Deep Infiltrating Endometriosis Surgery N/A
Active, not recruiting NCT05996809 - PMCF Study for COSEAL® in Gynecologic Surgery
Completed NCT05999162 - Mechanical Ileus in the Era of Minimally Invasive Colorectal Surgery
Not yet recruiting NCT05415059 - LEAFix Adhesion in Healthy Volunteers N/A
Active, not recruiting NCT03880435 - HYALOBARRIER® GEL ENDO Versus no HYALOBARRIER® GEL ENDO Following Operative Hysteroscopy for Improving Reproductive Outcome in Women With Intrauterine Pathology Wishing to Become Pregnant N/A
Completed NCT04669756 - Ovariopexy for Adhesion Prevention After Laparoscopic Removal of Endometriosis of the Pelvic Side Wall or the Ovary N/A