A Clinical Study Collecting Patients' Experience During Dental Implant Treatment
Launched by DR ROBERT BOWE · Nov 2, 2024
Trial Information
Current as of May 15, 2025
Not yet recruiting
Keywords
ClinConnect Summary
This clinical trial is focused on understanding patients' experiences during dental implant treatment. Researchers want to learn how patients feel before, during, and after receiving implants, whether for a single tooth, multiple teeth, or a full set. Participants will fill out questionnaires that ask about their acceptance and overall experience with the treatment. They will be monitored for up to one year after their final dental work.
To join the study, you need to be at least 18 years old and have a need for dental implants. You should be able to share your experiences and have a working email to receive information. It’s important that you can understand and answer questions in English. The study is not looking into the safety of the dental devices used, but rather focuses on collecting your feedback. Keep in mind that certain health conditions or situations, like pregnancy, might prevent you from participating. The trial is not yet recruiting participants, so there will be more information available soon.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Subject signed informed consent
- • Subject is at least 18 years old at the time of treatment
- • Subject presented with the need of dental implant treatment for single tooth, multiple teeth, or full-arch rehabilitation
- • Subject with medical and anatomical conditions that are in accordance with the applicable instructions for use (IFU)
- • Subject agree to provide information on her/his experience and outcomes before, during and after the treatment
- • Subject has a working e-mail address
- • Subject has sufficient English language skills for answering the PREM questionnaires
- Exclusion Criteria:
- • Anatomical conditions discovered during surgery preventing the use of intended implant system
- • Subject with history of allergy or adverse reactions to any materials used
- • Uncontrolled unstable systemic disease
- • Any ongoing application of medication that is interfering with the dental treatment
- • Subject is not willing / unable to complete the PREM questionnaires
- • Subject that is planning not to return to the investigational site for follow-up visits within study schedule
- • Pregnant or lactating women at the time of implant insertion
About Dr Robert Bowe
Dr. Robert Bowe is a distinguished clinical trial sponsor with extensive experience in the design and management of innovative research studies. With a strong background in clinical medicine and a commitment to advancing healthcare, Dr. Bowe collaborates with leading research institutions to facilitate the development of novel therapeutic interventions. His focus on rigorous scientific methodology and patient-centered approaches ensures the integrity and success of clinical trials, contributing to the advancement of medical knowledge and improved patient outcomes. Through his leadership, Dr. Bowe strives to bridge the gap between research and real-world application, fostering a collaborative environment that prioritizes both safety and efficacy.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Patients applied
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported