Evaluation of Bisphenol Release in Saliva after Remaining Adhesive Removal in Orthodontic Patients Using two different methods

Evaluation of Bisphenol Release in Saliva after Remaining Adhesive Removal in Orthodontic Patients Using Ultrasonic and Rotary Systems

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20200702047988N1

Enrollment

Registered

2020-08-26

Start date

2018-04-04

Completion date

Unknown

Last updated

2020-09-07

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

Conditions

Evaluation of bisphenol identified in saliva of orthodontic patients after debonding with two methods: Rotary system and ultrasonic scaler.

Interventions

Intervention 1: Intervention group1: Removing the adhesive with ultrasonic. Intervention 2: Intervention group 2: Removing the adhesive with rotary system.

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Patients with at least 16 bonded teeth in the mouth

Exclusion criteria

Exclusion criteria: Tobacco use Liver diseases Kidney diseases Taking drugs containing phenolic compounds

Design outcomes

Primary

Measure	Time frame
The amount of Bisphenol. Timepoint: End of treatment. Method of measurement: high-performance liquid chromatography/mass spectrometr device.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSara Seifi

Tabriz University of Medical Sciences

seifis@tbzmed.ac.ir+98 41 3335 5969

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 12, 2026