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Treatment Outcomes With Full Arch Rehabilitations Retained by Immediate or Conventionally Loaded Implants

Treatment Outcomes With Full Arch Rehabilitations Supported by Immediate or Conventionally Loaded Implants: A Randomized Clinical Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04930835
Acronym
ILOD
Enrollment
20
Registered
2021-06-18
Start date
2018-01-11
Completion date
2021-01-11
Last updated
2021-06-18

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

Conditions

Edentulous Jaw, Missing Teeth

Brief summary

This study aims to assess the treatment outcomes (clinical, functional and subjective) of full arch rehabilitations supported by implants with or without an immediate loading protocol. In this randomized clinical trial 20 fully edentulous patients were treated with full arch rehabilitations on dental implants. In half of the sample, the implants were loaded immediately by means of abutments after emplacement of the implant; but in the counterparts these abutments were connected to implants two months after the surgery (conventional protocol), and until that time the dentures were retained by healing abutments. Treatment outcomes were assessed at 2, 6 and 12 months after surgery. Clinical outcomes were quantified on the basis of implant failure rate, marginal bone loss and the peri-implant gingival index. Functional outcomes were calculated according to masticatory performance, estimated by the mixed fraction of a two-coloured chewing gum after 5, 10 and 15 chewing strokes, by the occlusal force recorded by pressure-sensitive sheets and by the bioelectrical muscular activity. The subjective outcomes of the treatment were assessed using both the oral satisfaction scale (visual analogue scale) and the Spanish version of the Oral Health Impact Profile (OHIP-20).

Interventions

PROCEDUREImplant supported dentures

Placement of dental implants with different loading protocols for supporting full arch dentures.

Sponsors

University of Salamanca
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Caregiver, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* completely edentulous individuals who had lacked teeth for more than 10 years, routine users of conventional complete prostheses. * sufficient amount of remaining bone to receive the implants in the region of the mandibular canines (minimum height=15 mm/minimum ridge width= 5mm) * no evidence of systemic or psychic pathology that might contraindicate the implant treatment.

Exclusion criteria

* Those in which oral surgery or cognitive evaluations are contraindicated

Design outcomes

Primary

MeasureTime frameDescription
MasticationOne year after treatmentMixing ability tests
Clinical Performance of Dental implantsOne year after treatmentImplant failure rate
Oral health-related quality of lifeOne year after treatmentimpact according to the OHIP-20 (Oral Health Impact Profile) instrument. The score range from 0 to 20, being 20 the worst outcome.
Area of Occlusal OcclusionOne year after treatmentAccording to pressure-sensitive colorimetric sheets it is recorded the area in square millimeters
Occlusal LoadOne year after treatmentAccording to the pressure-sensitive colorimetric sheets , the load in both the anterior and posterior region of the arch are calculated.

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026