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comparison of analgesic drug and laser effect on pain reduction after orthodontic separator implementation

Clinical comparison of Gelofen drug and low power diode laser effect on pain induced by orthodontic separator implementation

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016061316582N2
Enrollment
60
Registered
2016-10-31
Start date
2016-03-19
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

orthodontic pain. Disorder of teeth and supporting structures, unspecified

Interventions

Intervention 1: In drug group patients receive 400mg Gelofen an hour before placing separator between the contacts of maxillary molars and after placement using laser facade flash without therapeut
Treatment - Drugs
Treatment - Other
In drug group patients receive 400mg Gelofen an hour before placing separator between the contacts of maxillary molars and after placement using laser facade flash without therapeutic effect .
In the laser group patients receive placebo of the Gelofen an hours before placement of separator between the contacts of maxillary molars.Immediately after separator placement laser will expose to

Sponsors

Vice Chancellor for Research and Technology, Hamedan University of Medical Science
Lead Sponsor

Eligibility

Sex/Gender
All
Age
13 Years to 25 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Patients between13-25 years old;Female patients not to be pregnant; Patients with no orthodontic treatment history; Patients with no gelofen reaction history in the drug group; In the drug group the minimum weight should be 40 kg. Exclusion criteria: patients with history of systemic disease; Patients with periodontal disease, More than 3 mm Probing depth; Attached gingiva recession; Using antibiotic in drug group .

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
The pain after seprator placement. Timepoint: Immediately after the intervention, 6 hours after intervention, 12 hours after intervention, 24 hours after intervention,2 days after intervention,3 days or more after intervention. Method of measurement: Questionnaire Modified McGill.

Countries

Iran (Islamic Republic of)

Contacts

Public Contactvahid mollabashi

Hamedan University of Medical Sciences

vahidmolabashi@yahoo.com+98 81 3838 0130

Outcome results

None listed

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