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Assessing temperature _ controlled radiofrequency tonsil ablation and CO2- laser cryptolysis on treatment of chronic tonsillitis with caseum.

Assessing temperature _ controlled radiofrequency tonsil ablation and CO2- laser cryptolysis on treatment of chronic tonsillitis with caseum.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201303233186N3
Enrollment
50
Registered
2013-08-23
Start date
2013-05-22
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

Chronic tonsillitis with caseum. Chronic tonsillitis

Interventions

Intervention 1: Intervention : temperature _ controlled radiofrequency tonsil ablation. Intervention 2: Control : CO2- laser cryptolysis of tonsils.
Treatment - Other
Intervention : temperature _ controlled radiofrequency tonsil ablation
Control : CO2- laser cryptolysis of tonsils

Sponsors

Hamedan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criteria: patients upper than 18 years old referred to Besat Hospital clinic with chronic tonsillitis with caseum who had symptoms such as halitosis(with positive Finklestien smell test ) or feeling of foreign body and chronic irritation of tonsils; patients who had no periodontal disease, gingivitis or other systemic disease that result in halitosis such as hepatorenal and pulmonary and gastroenterological disease or diabetes mellitus , sinusitis, nasopharyngeal , oropharyngeal or laryngeal cancer in history and physical examination; patients who had no contraindications for radiofrequency of tonsils such as having cardiac pace maker, immunodeficiency disease or coagulation disorders and patients who had no limitation for CO2- laser. Exclusion criterion: cryptolysis such as anatomical orophryngeal anomalies or mallampati grading 3 or 4.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Halitosis. Timepoint: Before, 1 week, 1 month, 6 months after intervention. Method of measurement: Visual analog scale questionnaire.;Feeling of foreign body. Timepoint: Before, 1 week, 1 month,6 months after intervention. Method of measurement: Visual analog scale questionnaire.

Secondary

MeasureTime frame
Post intervension pain. Timepoint: 1, 3 and 7 days after intervension. Method of measurement: Visual analog scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFarnaz Hashemian

Hamedan University of Medical Sciences

hashemian@umsha.ac.ir+98 81 1264 0047

Outcome results

None listed

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