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The patient experience and clinical outcome of traditionally and computerized manufactured artificial teeth a comparison -An in-vivo study

Comparative evaluation of patient satisfaction and clinical efficiency with conventionally and digitally fabricated removable partial denture-A non-randomized crossover clinical trial - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/06/088568
Enrollment
20
Registered
2025-06-10
Start date
Unknown
Completion date
Unknown
Last updated
2025-06-24

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

Conditions

None listed

Interventions

Intervention1: Nil: Nil Intervention2: Nil: Nil

Sponsors

Dr Pranoti Ranit
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Kennedys Class I and Class II with sufficient inter-arch space verified by tentative jaw relation in patients with 25-60yrs old . and patients who are willing to participate in the study.

Exclusion criteria

Exclusion criteria: Patients with completely edentulous arch, Patients experiencing problems with mouth opening because of Temporomandibular disorders, patients with congenital or acquired defects in maxilla and mandible, Patients judged ineligible for inclusion criteria by principal investigator or designated contact person because of clinically significant medical or mental health findings.

Design outcomes

Primary

MeasureTime frame
To evaluate and compare patient satisfaction and clinical efficiency in conventionally fabricated removable partial denture and digitally fabricated removable partial denture nilTimepoint: 3 months

Secondary

MeasureTime frame
NilTimepoint: nil

Countries

India

Contacts

Public ContactDr Pranoti Ranit

Ranjeet Deshmukh Dental College.

dr.anujchandak@gmail.com9158192345

Outcome results

None listed

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