Pain, Discomfort, and Functional Impairments During Maxillary Expansion

Sponsor
Damascus University (Other)
Overall Status
Completed
CT.gov ID
NCT05248087
Collaborator
(none)
52
1
2
17.1
3

Study Details

Study Description

Brief Summary

Maxillary expansion is associated with varying degrees of pain and functional impairments. The current study aims to compare rapid maxillary expansion using a McNamara-type (bonded) appliance and slow maxillary expansion using a removable palatal expansion appliance concerning patient-centered outcomes. Those outcomes will include pain and discomfort, mastication difficulties, swallowing difficulties, and pressure on the soft tissues.

Condition or Disease Intervention/Treatment Phase
  • Device: The bonded McNamara-type appliance
  • Device: The removable palatal expansion appliance
N/A

Detailed Description

Skeletal maxillary constriction is one of the common orthodontic problems of all ages, which could be unilateral or bilateral. If it is neglected and not treated, it may result in later orthodontic problems such as skeletal deviation of the lower jaw. The current study aims to use two types of expanders to treat skeletal maxillary constriction in adolescents aged between 12 and 16 years. The study sample will include 52 patients who will be equally divided into two groups: the slow and the rapid maxillary expansion groups. Patients will be asked to answer a questionnaire within five assessment times during the expansion procedure. The questionnaire will contain four questions: 1) What is the degree of discomfort/pain? 2) What is the degree of mastication difficulties? 3) What is the degree of swallowing difficulties? 4) What is the degree of any sense of pressure in soft tissue?

Study Design

Study Type:
Interventional
Actual Enrollment :
52 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Assessment of Patient-centered Outcomes Associated With the Expansion of Skeletally Constricted Upper Jaw in the Adolescents Using Two Types of Expanders: A Randomized Controlled Trial
Actual Study Start Date :
Feb 20, 2020
Actual Primary Completion Date :
Mar 20, 2021
Actual Study Completion Date :
Jul 25, 2021

Arms and Interventions

Arm Intervention/Treatment
Experimental: The rapid maxillary expansion

The rapid maxillary expansion will be applied using a McNamara-type (bonded) appliance.

Device: The bonded McNamara-type appliance
The patient will be asked to expand twice a day until obtaining an overcorrection of 2-3 mm. Then the expander will be kept in place for three months as a retention period.

Active Comparator: The slow maxillary expansion

The slow maxillary expansion will be applied using a removable palatal expansion appliance.

Device: The removable palatal expansion appliance
The slow maxillary expansion will be applied using a removable palatal expansion appliance with a midline screw. The patient will be asked to expand twice a week until obtaining an overcorrection of 2-3 mm.

Outcome Measures

Primary Outcome Measures

  1. Change in the levels of discomfort or pain [T1: after 24 hours; T2: on the 7th day; T3: on the 15th day; T4: after 1 month; T5: after 4 months]

    The degree of pain and discomfort that patients feel will be determined using their answers to the following question (question 01): 'What is the degree of discomfort/pain?' The Visual Analogue Scale (VAS) will be adopted to measure the degree of discomfort/pain.

  2. Change in the levels of mastication difficulties [T1: after 24 hours; T2: on the 7th day; T3: on the 15th day; T4: after 1 month; T5: after 4 months]

    The degree of mastication difficulties that patients feel will be determined using their answers to the following question (question 02): 'What is the degree of mastication difficulties?' The Visual Analogue Scale (VAS) will be adopted to measure the degree of mastication difficulties.

  3. Change in the levels of swallowing difficulties [T1: after 24 hours; T2: on the 7th day; T3: on the 15th day; T4: after 1 month; T5: after 4 months]

    The degree of swallowing difficulties that patients feel will be determined using their answers to the following question (question 03): ' What is the degree of swallowing difficulties?' The Visual Analogue Scale (VAS) will be adopted to measure the degree of swallowing difficulties.

  4. Change in the levels of sensation of pressure on soft tissue [T1: after 24 hours; T2: on the 7th day; T3: on the 15th day; T4: after 1 month; T5: after 4 months]

    The degree of any sense of pressure in soft tissue that patients feel will be determined using their answers to the following question (question 04): ' What is the degree of any sense of pressure in soft tissue? ' The Visual Analogue Scale (VAS) will be adopted to measure the degree of any sense of pressure in soft tissue.

Eligibility Criteria

Criteria

Ages Eligible for Study:
12 Years to 16 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. Adolescents between 12 and 16 years.

  2. Early permanent dentition.

  3. Skeletal bilateral maxillary constriction.

  4. There is no loss or absence of any permanent teeth except for the third molar.

  5. Dental and skeletal class I/II malocclusion.

  6. Normal/mild vertical growth pattern.

Exclusion Criteria:
  1. Previous orthodontic treatment.

  2. A severe horizontal growth pattern.

  3. Any periodontal diseases.

  4. Any general diseases or syndromes.

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of Damascus Damascus Syrian Arab Republic

Sponsors and Collaborators

  • Damascus University

Investigators

  • Principal Investigator: Nancy Rabah, DDS,MSc, Specialist and Clinical Lecturer, Department of Orthodontics, University of Damascus
  • Principal Investigator: Heba M Al-Ibrahim, DDS,MSc, Specialist and Clinical Lecturer, Department of Orthodontics, University of Damascus
  • Study Chair: Mohammad Y Hajeer, DDS,MSc,PhD, Professor of Orthodontics, University of Damascus Dental School, Damascus, Syria
  • Study Chair: Rashad M.T. Murad, DDS,MSc,PhD, Professor of Pharmaceutics, University of Damascus, Faculty of Pharmacology, Damascus, Syria.

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Damascus University
ClinicalTrials.gov Identifier:
NCT05248087
Other Study ID Numbers:
  • UDDS-Ortho-02-2022
First Posted:
Feb 21, 2022
Last Update Posted:
Feb 21, 2022
Last Verified:
Feb 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 Damascus University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 21, 2022