TLX - comparison of 3D volumetric changes of the peri-implant soft tissue between 2 treatment protocols in the posterior mandible

Recruiting

• Conditions: implantation; K08.1; Loss of teeth due to accident, extraction or local periodontal disease

• Registration Number: DRKS00031178
• Lead Sponsor: Poliklinik für Zahnärztliche Chirurgie und Implantologie, Zentrum für Zahn-, Mund- und Kieferheilkunde (Carolinum) der Goethe-Universität Frankfurt am Main

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2023-02-02
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 46

Inclusion Criteria

Patients who have an indication for an implant-supported single crown in the lower posterior region
- Study participants must be informed about the follow-up appointments and must agree to present themselves at the clinic for the follow-up appointments
- The declaration of consent for voluntary participation in the study must be signed by the study participants before entering the study

Exclusion Criteria

- General contraindications for oral surgery and implantology, the medical history should not indicate any radiotherapy or chemotherapy due to malignant diseases within the last 4 years
- Smokers >20 cigarettes/day or consumers of cigarette-like products or tobacco chewers
- Taking medications that affect bone remodeling or soft tissue healing (e.g., steroids, antiresorptive drugs)
- Diseases that prevent patients from performing adequate oral hygiene
- Pregnant or lactating women

Study & Design

• Study Type: observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
3D Assessment: ROI (region of interest) (mm), mean volumetric change (linear) between different time points (preoperative, immediate postoperative, 3 and 6 months postoperative)-

Secondary Outcome Measures

Name	Time	Method
- Change of peri-implant soft tissue preoperative, immediate postoperative, 3 and 6 months postoperative<br>- mucosal recession<br>- probing depth<br>- Bleeding on probing (BOP)<br>- PROMs<br>- surgical time<br>- number of appointments befor final prosthetic delivery