Clinical trials

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Search and review clinical trials. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Risk Factors Associated With Infraposition of Implant Supported Single Crowns in the Anterior Maxilla

Losing a tooth in the front part of the upper jaw can affect both appearance and the ability to bite and chew. Treatment to replace missing teeth is therefore often required. Such treatment may be burdensome for the individual and can involve substantial costs for both the patient and society. A common treatment option is placement of a titanium screw (dental implant) in the jawbone. After a healing period, the implant is restored with a crown designed to resemble a natural tooth. Replacement of missing teeth with dental implants in the anterior maxilla can be particularly challenging. Over time, the crown of an implant may appear shorter than the adjacent natural teeth. This occurs because natural teeth may continue to change position throughout adulthood, whereas dental implants remain fixed within the bone. As a result, the implant-supported crown may appear to sink relative to neighboring teeth, a phenomenon referred to as infraposition. The prevalence of infraposition and the factors contributing to its development are not yet fully understood. The aim of this study is to determine the frequency and extent of infraposition and to identify potential contributing factors in individuals treated with a single implant-supported crown in the anterior maxilla. The study also aims to evaluate the aesthetic outcome after treatment from both the patient and the clinician perspective. The study hypothesis is that infraposition occurs in a clinically relevant proportion of patients and that certain factors, such as age at implant placement or individual dental characteristics, may increase the likelihood of its occurrence. It is further hypothesized that infraposition of the implant-supported crown may influence aesthetic appearance and that these changes may be perceived differently by patients and dental professionals. Through longitudinal follow-up and comparison of repeated digital scans, the study seeks to improve understanding of the occurrence of infraposition, its contributing factors, and its potential impact on the aesthetic outcome of implant-supported crowns over time.

Participants needed: 60
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Region VästerbottenUpdated: May 18, 2026Locations: 2
Eligibility criteria

Not listed

Status: Recruiting

Male Lichen Sclerosus - Risk Factors, Treatment, and Impact on Quality of Life

This observational study aims to evaluate routine treatment outcomes in men with lichen sclerosus (LS), including a long-term follow-up to assess disease progression and histopathological changes. The study also investigates potential risk factors for LS and the disease's impact on quality of life and sexual health.

Participants needed: 300
Trial details
Age: 18+Biological sex: MaleType: ObservationalSponsor: Region VästerbottenUpdated: Feb 10, 2026Locations: 1
Eligibility criteria

Biologically male [+11]

Age under 18 years old [+2]

Status: Recruiting

Evaluation of PSMA-PET and mpMRI in High-risk Prostate Cancer - Using Histopathologic Validation

In this trial the connection between image properties (mpMRI and PSMA-PET) and tissue properties (molecular and histopathology) will be investigated in order to improve diagnostics and image-based treatment guidance of prostate cancer.

Participants needed: 60
Trial details
Phase: Phase 3Age: 18+Biological sex: MaleType: InterventionalSponsor: Region VästerbottenUpdated: Mar 4, 2025Locations: 2
Eligibility criteria

Histologically confirmed prostate cancer planned to be treated with radical pros... [+8]

Non-MR-safe implants or another contraindication to MRI or PET [+9]

Status: Recruiting

Prognostic and Diagnostic Added Value of Medical Imaging in Gynecological Cancer (PRODIGYN)

The goal of this observational study is to learn about the added diagnostic and prognostic value of advanced medical imaging procedures in cervical cancer, endometrial cancer and ovarian cancer. The main questions it aims to answer are: * Does advanced medical imaging predict survival? * Can advanced medical imaging improve radiotherapy target planning? * Are advanced medical imaging results associated with risk markers found in tumor tissue? Participants will * Undergo four additional imaging procedures, as compared to clinical routine examinations, two at baseline and two after three months. * Be subject to clinical follow-up for five years.

Participants needed: 120
Trial details
Age: 18+Biological sex: FemaleType: ObservationalSponsor: Region VästerbottenUpdated: Dec 16, 2024Locations: 1
Eligibility criteria

Previously untreated primary cervical, endometrial, or strongly suspected epithe... [+3]

Imaging findings suggestive of other primary malignancy. [+2]