Improving the stability of the dental implants in the poor quality bone Oral Health
Conditions
Interventions
This study is a randomized controlled trial, including 2 groups of implants which will be placed in the same patients - the control group will receive conventional commercial implants, and the experim
Sponsors
Damascus University
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Patients with sufficient residual bone for conventional implant placement 2. Patients with bilateral Edentulous area in the maxilla 3. Patients displaying compliance with oral healthcare instructions and necessary visits
Exclusion criteria
Exclusion criteria: 1. Patients having undergone radiotherapy or with diseases such as osteoporosis that are a contraindication to implant placement 2. Patients with inadequate bone height and width available for implant placement and requiring horizontal or vertical bone augmentation 3. Medically compromised patients with systemic conditions that can impede implant stability and influence the treatment outcome
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Implant stability measured using the Mega ISQ Implant Stability Meter at 5 endpoints: (T0) immediately after surgery, (T1) 2 weeks, (T2) 4 weeks, (T3) 8 weeks, and (T4) 12 weeks | — |
Secondary
| Measure | Time frame |
|---|---|
| Insertion torque measured using a Torque Ratchet immediately after surgery for all implants | — |
Countries
Syria
Contacts
Public ContactMohammed;Mohammed Kattaa;Kattaa
;
Outcome results
None listed