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Clinical evaluation of the alignment efficacy and pain with CuNiTi and Multistranded SS arch wires during initial orthodontic treatment- Randomised clinical trial.

Clinical evaluation of the alignment efficacy and pain with CuNiTi and Multistranded SS arch wires during initial orthodontic treatment- Randomised clinical trial.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/02/031065
Enrollment
32
Registered
2021-02-08
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: - Health Condition 2: K006- Disturbances in tooth eruption

Interventions

Intervention1: 0.016inch Cu NiTi archwire: Copper nickel titanium wire used for decrowding of lower anterior teeth in the initial aligning and leveling phase. Control Intervention1: 0.0175 inch Multis

Sponsors

O Sobitha
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients of normal health with physical and mental fitness. 2. Age between 12 to 20 years 3. Patients with symmetrical jaws as assessed on orthopantamogram (OPG). 4. Confirmation that all permanent teeth have fully erupted from the second molar to second molar (with no extraction in the mandibular arch). 5. Mandibular anterior dental crowding (Littleâ??s irregularity index (Little 1975) greater than 6mm) 6. No spaces in the mandibular arch. 7. (Patients with class I molar and skeletal relationship) 8. Patients with normal vertical growth pattern. 9. Normal Systemic and periodontal health.

Exclusion criteria

Exclusion criteria: 1. Patients with systemic diseases or any drug therapy that interferes with orthodontic tooth movement. 2. Patients with any abnormal vertical growth pattern and horizontal growth pattern. 3. Patients with blocked out tooth in the lower anteriors. 4. Missing teeth except for third molars treatment with extractions (impacted or unerupted permanent teeth) 5. History of previous orthodontic treatment with either intra-oral or extra-oral appliances (including removable appliances, rapid palatal expansion appliances, or headgear) and functional appliances. 6. Craniofacial syndrome or Skeletal asymmetry (with cleft lip and palate, anomalies, and syndrome).

Design outcomes

Primary

MeasureTime frame
Assessment of Alleviation of Crowding, intercanine width, interpremolar width, inter molar width, littles irregularity score.Timepoint: preT0 (at the time of wire placement) and post treatment T6 (after 6 weeks)

Secondary

MeasureTime frame
Assessment of pain perceptionTimepoint: At 4hours (T1), 24hours (T2). 3days (T3), 1week (T4), 1 month (T5) and 6 weeks (T6)

Countries

India

Contacts

Public ContactS Gowri sankar

Narayana dental college and hospital

mandavabruno9@gmail.com9440976666

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026