A clinical trial to study and compare the fit and chewing effectiveness in lower denture retained using two different implant attaching systems.

Comparative Evaluation of effect of two attachment systems on retention and masticatory efficiency in patients receiving two implant retained mandibular overdenture: A randomized cross over clinical study. - nil

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2023/11/060387

Enrollment

Registered

2023-11-30

Start date

Unknown

Completion date

Unknown

Last updated

2023-12-19

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

Conditions

None listed

Interventions

Intervention1: two implant retained overdenture retained with ingeniously designed abutment-retention.sil attachment system: it is a modification of the stock abutment of any implant system into a bol

Eligibility

Inclusion criteria

Inclusion criteria: a.Completely edentulous participants requiring complete dentures b.Patients with moderately or poorly resorbed mandibular residual ridge. c.Patients indicated for implant retained overdenture in lower arch. d.Patient free from any systemic diseases that may affect osseointegration. e.Patients with normal temporomandibular joint movements. f.Patients with adequate inter-arch space. (22 mm and above) g.Patients willing for repeated visits and follow up.

Exclusion criteria

Exclusion criteria: a.Patients with mandibular edentulous ridges with undercuts. b.Patients with reduced salivary flow or having xerostomia. c.Patients with known allergy to denture base material. d.Patients undergoing radiotherapy, cancer therapy. e.Presence of systemic diseases producing oral manifestations. f.Patients having any surgical or congenital maxillofacial defects. g.Patients who are not willing to sign the consent form. h.Patients who are smokers or use tobacco in any form. i.Patients with neuromuscular disorders.

Design outcomes

Primary

Measure	Time frame
1.retention of overdentures 2.masticatory efficiencyTimepoint: 1.retention will be evaluated at baseline and after 3 months of overdenture wear 2.masticatory efficiency will be evaluated at baseline and after 3 months of overdenture wear	—

Secondary

Measure	Time frame
NILTimepoint: NIL	—

Countries

India

Contacts

Public ContactDr Pravisha Rai

K M Shah dental college and hospital

rajeshsethu77academics@gmail.com9725038434

Outcome results