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Comparision of Two Dentinal Densitizing Agents

Assessment Of Propolis, Dentin Bonding Agent And Placebo In Reducing Dentinal Hypersensity, In Hypersensitive Teeth Subsequent Of Periodontal Surgeries: A Randomized Clinical Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016102430475N1
Enrollment
120
Registered
2016-11-18
Start date
2016-01-07
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Dentinal Hypersensitivity. Other specified diseases of hard tissues of teeth

Interventions

Intervention 1: In group which treated with' Dentin Bonding Agent', light cure LED with 400-550 mW/cm2 power used for 15 seconds. Also application of placebo(distilled water) recommended after dryin
Treatment - Other
Treatment - Drugs
In group which treated with' Dentin Bonding Agent', light cure LED with 400-550 mW/cm2 power used for 15 seconds. Also application of placebo(distilled water) recommended after drying and isolation
In group which treated with '10% Propolis', placebo exposure was used after first application. So patients applied gel after drying and isolation of teeth by using disposable micro brush 2 times a d
In group which treated with '30% Propolis', placebo exposure was used after first application. So patients applied gel after drying and isolation of teeth by using disposable micro brush 2 times a da
In group which treated with 'Distilled Wather', placebo exposure was used after first application. So patients applied Distilled Wather after drying and isolation of teeth by using disposable micro b

Sponsors

Dentistry faculty,Tehran university of medical sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion Criteria: Patients who had periodontal surgery in Department of Periodontology in Dentistry Collegial of Tehran University; Patients who had maximum 2 not adjacent caries-free teeth with dentinal hypersensitivity at the cervical border; Patients with adequate and good oral hygiene; Patients with complete general and physical health . Exclusion Criteria: Patients who has any systemic illnesses and/or psychological diseases, and previous hospitalization; Teeth with dental caries, cracks or fractures in the cervical borders of the teeth; Teeth with any extensive and incorrect restorations,being of prostheses or orthodontic appliances; Patients who were drug addicted and analgesic and/or anti-inflammatory drugs users; Patients with a history of use of any desensitizing agents.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Dentinal Hypersensitivity. Timepoint: 1,7,14,21,60 and 90-day. Method of measurement: Visual Analog Scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMelika Zargar

Dentistry faculty, Tehran University Of Medical Sciences

Zargar.Melika@yahoo.com+98 21 5585 1131

Outcome results

None listed

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