NCT04606745

Brief Summary

A common goal of the health professions is to keep the elderly functional, preventing sarcopenia and frailty. Is there an association between handgrip strength in partially edentulous elderlies after completing their dentition with removable partial dentures?

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
60

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Oct 2018

Typical duration for all trials

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

October 1, 2018

Completed
2.1 years until next milestone

First Submitted

Initial submission to the registry

October 22, 2020

Completed
6 days until next milestone

First Posted

Study publicly available on registry

October 28, 2020

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2020

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

January 31, 2021

Completed
Last Updated

October 28, 2020

Status Verified

October 1, 2020

Enrollment Period

2.3 years

First QC Date

October 22, 2020

Last Update Submit

October 22, 2020

Conditions

Sarcopenia

Keywords

removable partial dentures

Outcome Measures

Primary Outcomes (1)

  • Handgrip strength

    role of use of removable partial dentures (RPD) in handgrip strength in octogenarians

    18 months

Eligibility Criteria

Age80 Years+
Sexall
Healthy VolunteersYes
Age GroupsOlder Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Independent octogenarians that consulted in centers of the greater metropolitan area of Santiago, Chile, in search of solving their lack of posterior teeth with dental prostheses

You may qualify if:

  • agree to participate by signing the voluntary informed consent form
  • qualify according to the Eichner Index in any of the categories that represent the loss of premolars and molars: B3-B4-C1-and C2.

You may not qualify if:

  • not accepting to participate
  • cognitive or auditory sensory impairment-
  • being dependent in activities of daily living
  • belonging to another category of the Eichner Index

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Universidad de Chile

Santiago, Chile

Location

MeSH Terms

Conditions

Sarcopenia

Condition Hierarchy (Ancestors)

Muscular AtrophyNeuromuscular ManifestationsNeurologic ManifestationsNervous System DiseasesAtrophyPathological Conditions, AnatomicalPathological Conditions, Signs and SymptomsSigns and Symptoms

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Target Duration
18 Months
Sponsor Type
OTHER GOV
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
MD

Study Record Dates

First Submitted

October 22, 2020

First Posted

October 28, 2020

Study Start

October 1, 2018

Primary Completion

December 31, 2020

Study Completion

January 31, 2021

Last Updated

October 28, 2020

Record last verified: 2020-10

Locations

CL(1)