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Comparison of Alignment Speed, Patient Discomfort and Root Resorption Between Two Different Sequences of Archwires

Comparison of Alignment Speed, Patient Discomfort and Root Resorption Between Two Different Sequences of Archwires

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07758556
Enrollment
60
Registered
2026-08-11
Start date
2024-12-20
Completion date
2025-09-02
Last updated
2026-08-13

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

Conditions

External Root Resorption, Pain, Speed of Alignment

Brief summary

In this Clinical trial we aim to compare alignment speed, patient discomfort and root resorption between two different sequences of NiTi archwires

Detailed description

This study will establish and evaluate a set of alignment wires that is efficient in terms of reduced number of patient's visits, yet periodontally safe and acceptable in terms of patient discomfort.

Interventions

DEVICEArchwire

NiTi Archwires will be used for tooth alignment

Sponsors

Foundation University Islamabad
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Masking description

Participants will have no idea which group of archwires they are included in

Eligibility

Sex/Gender
ALL
Age
12 Years to 35 Years
Healthy volunteers
No

Inclusion criteria

Age range 12-35 years. * Both male and female patients. * Medically-fit patients with no medical condition associated with root resorption risk. * No previous history of orthodontic treatment. * Patients requiring complete upper and lower orthodontic treatment with fixed appliance. * Angle class I, II, and III malocclusion with crowding in both maxillary and mandibular anterior dentition. * Healthy permanent dentition with adequate oral hygiene and no periodontal diseases; before the start of orthodontic treatment.

Exclusion criteria

Cleft lip \& palate patients * Syndromic patients * Patients with bone pathologies * Habits such as smoking * Patients with parafunctional habits or history of pre-existing root resorption * Patients taking drugs which inhibit or accelerate tooth movement * Tooth or teeth with periapical infection. * Patients with pain from any other medical or dental condition that may have affected their reported discomfort scores were excluded * Endodontically treated mandibular or maxillary anterior teeth * Presence of blocked-out tooth that did not allow for placement of the bracket or full AW engagement at the initial bonding.

Design outcomes

Primary

MeasureTime frameDescription
Speed of alignment6 monthsSpeed of alignment will be calculated in terms of number of visits and measured by Littles irregularity Index in millimeters

Secondary

MeasureTime frameDescription
Patient discomfort6 monthsWill be measured as scoring on pain proforma on Visual analogue scale

Countries

Pakistan

Contacts

STUDY_CHAIRShoaib Rahim, FCPS

FUCD & H

STUDY_CHAIRRozina Nazir, FCPS

FUCD & H

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 14, 2026