Retention

4

Review clinical trials related to Retention. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Comparative 3-dimensional Superimposition Analysis of Dentition in Horizontal and Vertical Grower During the Retention Phase -A Prospective Clinical Trial''

This study aims to investigate the relationship between facial type and relapse of dentition post-orthodontically during the retention phase. According to the retention theorem "teeth which have been moved through orthodontic treatment tend to naturally return to their original position. It is hypothesized that significant differences will exist in tooth movement patterns between horizontal and vertical growers, with horizontal growers exhibiting more pronounced tooth movement in the vertical plane particularly in the overbite as compared to the vertical growers . Furthermore, it is expected that facial type will influence the stability of orthodontic treatment outcomes, with long-faced individuals showing more relapse of mandibular incisor alignment and crowding. By exploring this relationship, this study aims to provide valuable insights into the factors influencing orthodontic treatment outcomes and stability. With long-faced individuals exhibiting more mandibular backward rotation and short-faced individuals showing forward rotation, which increases the risk of deep bite . Additionally, understanding these factors is crucial for orthodontists to predict and prevent potential relapse, ensuring optimal treatment results and long-term stability. Hence, the present trial will be undertaken to assess the changes and compare If there is any difference in tooth movement in 3-Dimensional superimposition in the dentition in horizontal and vertical growers post orthodontically over a period of retention phase.

Participants needed: 44
Trial details
Age: 18-45Biological sex: AllType: InterventionalSponsor: Postgraduate Institute of Dental Sciences RohtakUpdated: Jun 3, 2026Locations: 1
Eligibility criteria

Fixed orthodontic cases with FMA of 26 0 or more for hyperdivergent cases and FM... [+5]

Subjects with incomplete orthodontic treatment. [+6]

Status: Not yet recruiting

3D Printed vs. Milled Occlusal Splints in Dentistry

This crossover study aims to evaluate the wear comfort, retention, and stability of 3D-printed and milled occlusal splints in healthy subjects. The main question it aims to answer is: Research questions \- How do healthy subjects experience the wear comfort, fitting, retention and stability of a printed and milled occlusal splint? and how do clinicians experience the fitting, retention and stability of the splints? By systematically assessing self-reported outcomes, this research seeks to contribute valuable insights into the practical applications of both technologies. The findings may not only enhance our understanding of patient preferences but also guide future developments in the design and manufacturing of occlusal splints, ultimately improving patient care in dental practice.

Participants needed: 24
Trial details
Age: 18-45Biological sex: AllType: ObservationalSponsor: Radboud University Medical CenterUpdated: Nov 19, 2025Duration: 6 Weeks
Eligibility criteria

Subjects being healthy (ASA <IV) [+3]

Subjects with dental issues other than the inclusion criteria [+5]

Status: Recruiting

Clinical Trial Recruitment and Retention Strategies for Family Members in the ICU

There is a need to identify strategies that improve the conduct of clinical trials involving family members of intensive care unit (ICU) patients. The purpose of the present study is to evaluate recruitment and retention strategies for clinical trials involving family members of ICU patients. 4 strategies (2 recruitment and 2 retention) will be tested. Investigators will integrate the strategies into three existing studies that involve family members of ICU patients. Participants will be randomized using a 2x2 factorial design. The co-primary outcomes are recruitment percentage (participants enrolled/participants approached) and retention percentage (participants completing follow-up/participants enrolled).

Participants needed: 160
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Lady Davis InstituteUpdated: Jun 4, 2025Locations: 1
Eligibility criteria

Has family member admitted to an intensive care unit. [+2]

Has another family member participating in the trial [+1]

Status: Recruiting

Restoration of Non-carious Cervical Lesions With Different Resin Composites and Universal Adhesive

patients with non carious cervical lesions suffer from dentin sensitivity and presence of cavitations and gingival recession. Restoring these lesions with different composites and evaluation of restorations every 6 months will be done to know the effect of different composite types and consistencies in retention of restorations of such lesions.

Participants needed: 52
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Ain Shams UniversityUpdated: Feb 27, 2025Locations: 1
Eligibility criteria

Presence of at least 2 NCCLs in one side. [+4]

Medically compromised patients. [+6]