Exploration of Patient Satisfaction with an Implant Protocol Utilizing Cooling-Free and Slow Drilling for Immediate Implants with Immediate Loading. A Prospective Questionnaire Study.

Exploration of Patient Satisfaction with an Implant Protocol Utilizing Cooling-Free and Slow Drilling for Immediate Implants with Immediate Loading. A Prospective Questionnaire Study. - PQN1vsRCC

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00033271

Enrollment

Registered

2024-04-02

Start date

2025-12-08

Completion date

Unknown

Last updated

2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Necessary immediate single implant placement in the maxillary esthetic zone (Teeth 14-24)

Interventions

Group 1: Patients from the intervention study DRKS00033328 who underwent immediate implantation and immediate restoration with either the implant system (N1™ System, Nobel Biocare® AB, Gothenburg, Swe

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients meeting the indication for immediate implantation of a single-tooth implant in the upper jaw front. Healthy patients without severe systemic diseases. Patients with sufficient bone volume for implantation. Willingness to participate in the study and capacity to provide informed consent.

Exclusion criteria

Exclusion criteria: Patients with severe bone or tissue defects. Previous participation in similar studies or previous implantation or augmentation in the treatment area. Known allergies to materials associated with the implants. Patients with severe systemic diseases such as uncontrolled diabetes or autoimmune disorders.

Design outcomes

Primary

Measure	Time frame
Evaluation of patient experience during implantation through questions about disruption caused by drilling noises and water during the procedure. When will this parameter be assessed: Directly after the operation How is this done: Directly after the operation: Capturing the implantation experience immediately after the procedure using a structured questionnaire specifically addressing the mentioned disruptive factors.	—

Measure

Time frame

Evaluation of patient experience during implantation through questions about disruption caused by drilling noises and water during the procedure. When will this parameter be assessed: Directly after the operation How is this done: Directly after the operation: Capturing the implantation experience immediately after the procedure using a structured questionnaire specifically addressing the mentioned disruptive factors.

—

Secondary

Measure	Time frame
Assessment of overall patient satisfaction with implantation and immediate restoration by capturing their satisfaction and perception. When will this parameter be assessed: Before the operation and during the follow-up How is this done: Before the operation and during the follow-up: Utilizing a standardized questionnaire to evaluate overall patient satisfaction and perception both before the commencement and after the completion of the treatment.	—

Measure

Time frame

Assessment of overall patient satisfaction with implantation and immediate restoration by capturing their satisfaction and perception. When will this parameter be assessed: Before the operation and during the follow-up How is this done: Before the operation and during the follow-up: Utilizing a standardized questionnaire to evaluate overall patient satisfaction and perception both before the commencement and after the completion of the treatment.

—

Countries

Austria

Contacts

Public ContactRebecca Rosen

Akademie für Orale Implantologie

rosen.rebecca@me.com+43 1 402 86 68

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Aug 9, 2026