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â??Simpli5yâ?? concept of Full-mouth rehabilitation.

â??Simpli5yâ?? A noval concept for implant supported fixed rehabilitation of completely edentulous maxillary and mandibular arches

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/10/028548
Enrollment
100
Registered
2020-10-22
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: R99- Ill-defined and unknown cause of mortality

Interventions

Intervention1: Dental implant: Surgical placement of dental implant in maxillary and mandibular arch Intervention2: Dental implant,restoration: immediate loading, type of restoration Control Intervent

Sponsors

Rajiv Gandhi University of health science
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1) Complete arch edentulous in both maxillary and mandibular arches 2) Patients who were wearing conventional complete denture in maxillary and mandibular arch and those who were not 3) Patients in whom the available bone height was a minimum of 14-16 mm and width of 5mm of width 4) Patients who had an adequate inter-arch space of 14-18mm. 5) A patient who agreed for a follow-up of 5 years.

Exclusion criteria

Exclusion criteria: 1) Patients in whom immediate extraction and placement of implants was carried out. 2)Those patients in whom the grafting procedure was required. 3) Patients with bone diseases. 4) Patients who wanted an overdenture 5) Patients who wished to have more than 3 implants in the maxillary arch and 2 implants in mandibular arch for full arch restoration, respectively.6) Patients with Unrealistic expectations, unable to commit for follow-up.

Design outcomes

Primary

MeasureTime frame
primary outcome measures, implant survival and prosthetic survival were evaluated based the long-term survival. Implant survival included clinical stability, patient-reported function without any discomfort, infection, and absence of suppuration or radiolucent areas around the implants at 5-year post-surgicallyTimepoint: primary outcome measures, implant survival and prosthetic survival were evaluated based the long-term survival. Implant survival included clinical stability, patient-reported function without any discomfort, infection, and absence of suppuration or radiolucent areas around the implants at 5-year post-surgically

Secondary

MeasureTime frame
Secondary outcome measures were checked for the marginal bone level and incidence of complications. The marginal bone level was evaluated at 5 years of function in comparison with that of baseline reading recorded at the time of restoration. Marginal bone was measured using the digital image of an intraoral radiograph of each implant region, and assessment was done in the Carestream software.Timepoint: 5 years

Countries

India

Contacts

Public ContactRamesh chowdhary

Rajarajeswari Dental college

drramc@yahoo.com

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026