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Effectiveness of Two Types of Fixed Lingual Retainers in Preventing Mandibular Incisor Relapse

D

Dow University of Health Sciences

Status

Completed

Conditions

Relapse

Treatments

Device: Orthodontic retainers

Study type

Interventional

Funder types

Other

Identifiers

NCT03881813
DUHS/DR-0/2017/327

Details and patient eligibility

About

The study evaluates effectiveness of two types of fixed retainers in post orthodontic patients. Half of the subjects are randomly allocated Group 1 retainer (FRC) and other half is given Group 2 retainer (MSW) and followed for a period of one year.

Full description

54 subjects were recruited and divided into two groups by random allocation. Consents were obtained . Group 1 received fiber reinforced composite retainer and group 2 received multistranded stainless steel wire retainer. The patients were recalled at every three months interval for a period of 12 months. They were evaluated for number of fractures, failure pattern based on adhesive remnant index and relapse tendency by measuring little's irregularity index.

Enrollment

54 patients

Sex

All

Ages

14 to 30 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Subjects who have completed fixed appliance orthodontic treatment.
  • Subjects who have signed the consent forms.
  • Subjects who have accepted the terms and conditions of visiting after every three months for one year.
  • Non extraction cases in the mandibular arch with no IPR.
  • Patients without caries/ restoration/ fracture on the lower anterior teeth.
  • Patients with healthy periodontium with no periodontal disease at that time.

Exclusion criteria

  • Presence of syndrome or systemic disease.
  • Patients taking medications/ drugs.
  • Patients with poor oral hygiene.
  • Patients with congenitally absent/ missing anterior teeth in the mandibular arch.
  • Patients with habit of clenching/ bruxism.
  • Patients with history of betel nut chewing.
  • Presence of occlusal interferences.

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

54 participants in 2 patient groups

Fiber reinforced composite retainers
Experimental group
Description:
Fiber reinforced composite retainers were inserted in group 1 and were evaluated after every 3 months for a follow up period of 3 months.
Treatment:
Device: Orthodontic retainers
Multistranded stainless steel retainers
Experimental group
Description:
Multistranded stainless steel retainers were inserted in group 2 and were evaluated after every 3 months for a follow up period of 3 months.
Treatment:
Device: Orthodontic retainers

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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