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A clinical study on tooth movement and identifying the factors influencing it in patients with irregular teeth.

Evaluation of tooth movement and identify the factors influencing it during canine distal movement with and without orthodontic stress in malocclusion patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2018/05/013700
Enrollment
24
Registered
2018-05-04
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: null- MALOCCLUSION

Interventions

Intervention1: orthodontic intervention with standardized stress for maxillary canine.: The standardized stress of 52kPA will be given for a period of 84 days. Control Intervention1: orthodontic inter

Sponsors

Dr S LALITHAPRIYA
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Angleâ??s class I & II malocclusion that requires segmental maxillary canine retraction 2. There should be no intra- arch canine interference 3. Canine mesial Angulation 11degrees +/- 10 degrees. 4. Eruption of all permanent teeth in the both arch. 5. Absence of congenital missing of any permanent teeth except third molar. 6. Third molar might be missing/fully erupted/partially erupted/impacted. 7. Patients who needs extraction of either all first 1st premolars or only upper 1st premolars for therapeutic purpose. 8. Absence of aberrant morphology of roots. 9. Absence of craniofacial malformation. 10. Absence of any supernumerary/supplementary teeth.

Exclusion criteria

Exclusion criteria: 1. History of facial/dental trauma. 2. Root canal treated maxillary canine. 3. Crown and bridge in the upper anterior teeth. 4. Ectopically erupted canine. 5. Systemic disease that requires regular monitoring and medicine intake. 6. Presence of periodontitis. 7. Deleterious oral Habits. 8. Pregnant and lactating women 9. Patients who are currently taking or recently taken NSAIDâ??S, Ibandronates, vitamin D, Relaxin, Calcium, PTH, Progesterone, Insulin, Estrogen, Prostaglandins and Corticosteroids. 10. Patients under medication for hormonal disorders. 11. No history of use of analgesics within the last 3 days before the procedure. 12. Patients with known allergic to nickel.

Design outcomes

Primary

MeasureTime frame
Amount and type of tooth movement.Timepoint: Days 0,7th,28th,56th and 84th.

Secondary

MeasureTime frame
Alveolar bone densityTimepoint: days 0 and 84th;Expression level of interleukin â?? 1 beta in Gingival crevicular fluid.Timepoint: Before appliance placement-zero hour, After appliance placement- 1hr, 24hr, 7th day,28th day, 56th day and 84th day.;Pain intensityTimepoint: Before appliance placement-zero hour, After appliance placement- 1hr, 24hr, and followed for 7 days.;The incidence of root resorption.Timepoint: 0 and 84th day

Countries

India

Contacts

Public ContactProf Dr K RAJASIGAMANI

Rajah Muthiah Dental college and hospital

pr.lallu@yahoo.co.in9843644114

Outcome results

None listed

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