None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1.Patients with completely edentulous arch or arch with non-restorable teeth requiring extraction to achieve complete edentulism. 2.No acute infection is present. 3.Patients with good oral hygiene. 4.Patients willing to participate and provide informed and signed consent. 5.Patients who were willing to report for follow-up visits. 6.Patients with adequate hearing ability and those who did not use or require any hearing aid.
Exclusion criteria
Exclusion criteria: 1.Patients with history of any chronic illness (any systemic disease), tobacco intake (smoke or smokeless) , alcoholism or any other substance abuse, temporomandibular disorders, or Bruxism and any other parafunctional habits like clenching, tongue thrusting, etc. 2.Patients with neurological disorders affecting brain function. 3.Patients with severe cognitive impairment. 4.Patients with inadequate bone quality/quantity for implant placement. 5.Active chemotherapy or active radiotherapy. 6.Use of medications affecting neuromuscular activity, e.g., neuroleptics or antidepressants.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To evaluate cortical brain activity using ElectroEncephaloGram [EEG], Active Tactile Sensibility [ATS], and to assess Oral Health Related Quality of Life using a validated OHIP-14 index, and to compare and correlate the above parameters among patients treated with complete dentures versus implant prosthesis and within same patients before with complete dentures; and after i.e. with implant prosthesis. Timepoint: At 1 week, 1 month, and 3 months post prosthesis installation. | — |
Secondary
| Measure | Time frame |
|---|---|
| NILTimepoint: NIL | — |
Countries
India
Contacts
Faculty of Dental Sciences, Institute of Medical Sciences, Banaras Hindu University