The Effectiveness of Combined Design Nance/Transpalatal Arch Appliance in Maintaining Arch Dimensions After Premature Extraction of Primary Molars

Sponsor
Alexandria University (Other)
Overall Status
Completed
CT.gov ID
NCT05514145
Collaborator
(none)
30
1
2
15.9
1.9

Study Details

Study Description

Brief Summary

This study will evaluate the effectiveness of N-TPA appliance compared to Nance SM in maintaining the arch dimensions after bilateral premature extraction of primary molars in children.

Condition or Disease Intervention/Treatment Phase
  • Device: Nance/Transpalatal arch space maintainer
  • Device: Nance space maintainer
N/A

Detailed Description

In this randomized controlled clinical trial, 30 healthy children, 8-9 years of age with premature extraction of bilateral maxillary primary molars will be selected. Children will be randomly allocated into two equal groups of 15 children each according to the type of the appliance that will be used. Group I will receive a a Nance SM, and Group II a combined N-TPA appliance . Panoramic X-rays and study casts will be made, and baseline measurements will be recorded including arch circumference, intermolar width and arch depth. The appliances will be fabricated and cemented intra-orally.

The patients will be followed up at 3, 6 and 9 months for re-evaluation of arch circumference, intermolar width, arch depth, and patient acceptance.

Study Design

Study Type:
Interventional
Actual Enrollment :
30 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Randomized parallel controlled clinical trialRandomized parallel controlled clinical trial
Masking:
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose:
Prevention
Official Title:
The Effectiveness of Combined Design Nance/Transpalatal Arch Appliance in Maintaining Arch Dimensions After Premature Extraction of Primary Molars (Randomized Controlled Clinical Trial)
Actual Study Start Date :
Jan 1, 2021
Actual Primary Completion Date :
May 1, 2022
Actual Study Completion Date :
May 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Nance space maintainer

Conventional space maintainer for the maxillary arch as control

Device: Nance space maintainer
Conventional space maintainer for the maxillary arch used in mixed dentition

Experimental: Nance/Transpalatal arch space maintainer

New design of a space maintainer for the maxillary arch

Device: Nance/Transpalatal arch space maintainer
A combined design of both Nance and Transpalatal arch space maintainers as a space maintainer for the maxillary arch in mixed dentition

Outcome Measures

Primary Outcome Measures

  1. Efficacy in maintaining arch dimensions [9 months]

    All arch dimensions are measured with a 0.5 mm stainless steel wire on the study casts which was then measured with a digital caliper in millimeters (accuracy up to 0.02mm): Changes in arch circumference after insertion of both Nance and Nance/transpalatal arch (N-TPA) appliances after 3, 6- and 9-months follow-up. Changes in intermolar width after insertion of both Nance and Nance/transpalatal arch (N-TPA) appliances after 3, 6- and 9-months follow-up. Changes in arch depth after insertion of both Nance and Nance/transpalatal arch (N-TPA) appliances after 3, 6- and 9-months follow-up.

Secondary Outcome Measures

  1. Patient acceptance by modified faces pain scale [9 months]

    Patient acceptance are measured by the modified faces pain scale of both Nance and N-TPA appliances after 3, 6- and 9-months follow-up. Patient acceptance is measured as : (a) Satisfied (b) Indifferent (c) Dissatisfied

Eligibility Criteria

Criteria

Ages Eligible for Study:
8 Years to 9 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Fully erupted maxillary permanent first molars.

  • Angle's class I occlusion.(31)

  • Adequate space for premolar eruption according to Moyer's arch length analysis.(31)

  • Fair to good oral hygiene according to Silness and Loe plaque index.(32)

  • No history of allergy to polymethyl methacrylate.

Exclusion Criteria:
  • Children with congenitally absent permanent successors.

  • Children with successors not covered by bone with 2/3 of the root formed.(33)

Contacts and Locations

Locations

Site City State Country Postal Code
1 Faculty of dentistry, Alexandria University Alexandria Egypt

Sponsors and Collaborators

  • Alexandria University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Sara Ahmed Elsayed, MSc student, Alexandria University
ClinicalTrials.gov Identifier:
NCT05514145
Other Study ID Numbers:
  • 301015
First Posted:
Aug 24, 2022
Last Update Posted:
Aug 24, 2022
Last Verified:
Aug 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Sara Ahmed Elsayed, MSc student, Alexandria University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 24, 2022