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Therapeutic and analgesic efficacy of laser in conjunction with pharmaceutical therapy for trigeminal neuralgia

Therapeutic and analgesic efficacy of laser in conjunction with pharmaceutical therapy for trigeminal neuralgia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201601142464N15
Enrollment
30
Registered
2016-12-23
Start date
2015-04-21
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

Trigeminal neuralgia. Syndrome of paroxysmal facial pain Tic douloureux

Interventions

Intervention 1: Intervention Group: Laser treatment with medication Medication: Tablets 200 mg orally, once a day for three months Laser: GaAlAS diode laser with a wavelength of 810 nm, continus form
Treatment - Drugs
Intervention Group: Laser treatment with medication Medication: Tablets 200 mg orally, once a day for three months Laser: GaAlAS diode laser with a wavelength of 810 nm, continus form, dose 6.36
Control group: Medication with sham laser Medication: Carbamazepine, tablets, 200 mg orally, once a day for three months Laser: Sham laser

Sponsors

Dental Research Center, Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criteria: Patients with definite diagnosis of TN according to the criteria of the International Headache Society (IHS) were included [HIS 3 with ICD-10 (G44.0) coding]; Patients who were under standard pharmaceutical treatment for TN but had not experienced any improvement were also included. Exclusion criteria: pregnancy Patients

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Compare the severity of pain. Timepoint: Before treatment - Upon completion of treatment- At two months after completion of treatment. Method of measurement: Visual Analog Scale.

Secondary

MeasureTime frame
The side effects of the drug include dizziness. Timepoint: Before treatment- Upon completion of treatment-At two months after completion of treatment. Method of measurement: According patient.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Shamsoulmolouk Najafi

Tehran University of Medical Sciences / School of Dentistry, Tehran University of Medical Sciences I

najafi_drsh@yahoo.com+98 21 5585 1149

Outcome results

None listed

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