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Comparison of Different Methods of Controlling Pain During Debonding of Orthodontic Brackets

A

Armed Forces Institute of Dentistry, Pakistan

Status

Completed

Conditions

Orthodontic Appliance Complication
Analgesia

Treatments

Other: Stabilization of teeth during debonding using fingure pressure and elastic wafer

Study type

Interventional

Funder types

Other

Identifiers

NCT05104190
Orthodontic pain

Details and patient eligibility

About

Purpose of this study was to evaluate different methods of controlling pain during debonding

Full description

Patients data was obtained from the Department of Orthodontics, Armed Forces Institute of Dentistry, Rawalpindi. One Hundred and ten patients were included in the study, which were divided into two groups, 55 patients in each group, based on method of controlling pain during debonding. To control pain during debonding in one group , teeth were stabilized with finger pressure with cotton between finger and teeth and then debonding using open mouth technique was done. In second group teeth were stabilized using a plastic wafer between maxillary and mandibular teeth and then debonding was done using closed mouth technique. In order to reduce biasness, all of the patients were debonded with same plier and with wires still ligated to brackets. With the help of VAS, pain score was measured after debonding. A single operator performed complete procedure of debonding and pain recording.

Enrollment

148 patients

Sex

All

Ages

13 to 21 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Patients between 13-21 years of age who can understand, assess, and answer the questionnaires. 2) No missing teeth except extracted premolars 3) Undergoing upper and lower fixed orthodontic treatment with Roth prescription 0.022-inch metal brackets . 4) Finishing arch wires present for at least two months

Exclusion criteria

  1. The subjects with a previous history of facial or mandibular surgery or syndromes affecting the jaw or face .
  2. Patient with history of jaw sugeries.
  3. Patients with history of taking medicine periodically or in the last 24 hours (eg, painkillers, corticosteroids, and antiflu drugs),
  4. Patient with history of debonded brackets and replacement.
  5. Patient with history of tooth transplantation or microscrews placement.

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

148 participants in 2 patient groups

plastic wafers group
Experimental group
Description:
In one arm/ group 1 (plastic wafers group), debonding was done by open mouth technique. All brackets were removed using same plier i.e. angled direct bracket remover. Figure pressure in the apical direction was applied concomitantly applied to stabilize each tooth. Loose cotton was used between thumb and tooth during debonding. Arch wires and ligatures were not removed during debonding. Patient pain score during procedure was measured using visual analogue scale ranging from zero to one hundred (0-100) In
Treatment:
Other: Stabilization of teeth during debonding using fingure pressure and elastic wafer
finger pressure group
Experimental group
Description:
In another arm/ group 2( finger pressure group) brackets were removed in the same way with the same debonding plier as in group 1 but soft acrylic sheets folded 4 times were placed between upper and lower dentition with the patient biting on this wafer. Wires and ligatures were left tied to brackets during debonding. After the procedure, patient was asked about pain using visual analogue scale.
Treatment:
Other: Stabilization of teeth during debonding using fingure pressure and elastic wafer

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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