ClinicalTrials.Veeva

Menu

Pulpal Blood Flow Changes Using SuperElastic 0.018-inch Nickel Titanium

J

Jordan University of Science and Technology

Status

Completed

Conditions

Orthodontic Appliance

Treatments

Procedure: 0.014-inch NiTi on one side /0.018-inch NiTi on the other side
Procedure: 0.016-inch NiTi on one side /0.018-inch NiTi on the other side

Study type

Interventional

Funder types

Other

Identifiers

NCT04378205
39/2018

Details and patient eligibility

About

to record pulpal blood flow (PBF) changes associated with using 0.018-inch Nickel Titanium (NiTi) as the first alignment archwire during fixed orthodontic treatment.

Full description

Forty healthy patients with lower arch mild crowding with less than 2mm contact point displacement at any teeth were included. A split mouth study design was applied. Where each patient received 2 archwire sizes at one time joined in the midline by crimpable hook and applied in the lower arch.

Patients were assigned into one of 2 groups based on archwire sizes used. Group (1); 0.014-inch and 0.018-inch NiTi and Group (2); 0.016-inch and 0.018-inch NiTi. A Laser Doppler Flowmeter was used to measure PBF at different time intervals (T0-T5).

Enrollment

40 patients

Sex

All

Ages

18 to 25 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • age 18-25 years
  • Class I skeletal malocclusion
  • Mild lower arches crowding.
  • Contact point displacement less than 2 mm.
  • No previous orthodontic treatment

Exclusion criteria

  • Missing teeth
  • Poor oral hygiene
  • deep carious teeth
  • history of previous trauma
  • any medical conditions affecting blood vessels
  • smokers

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

40 participants in 2 patient groups

0.014/0.018 NiTi arch wire
Experimental group
Description:
0.014-inch NiTi on one side /0.018-inch NiTi on the other side (Nitinol SuperElastic 3M, Unitek) for initial alignment. This group included 20 patients
Treatment:
Procedure: 0.014-inch NiTi on one side /0.018-inch NiTi on the other side
0.016/0.018 NiTi arch wire
Experimental group
Description:
0.016-inch NiTi on one side / 0.018-inch NiTi on the other side (Nitinol SuperElastic 3M, Unitek) for initial alignment. This group included 20 patients
Treatment:
Procedure: 0.016-inch NiTi on one side /0.018-inch NiTi on the other side

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems