Comparision of Adenidectomy versus Adenotonsillectomy on changing in symptoms in patients less than 14 years old with chronic rhinosinositis

Comparision of Adenidectomy versus Adenotonsillectomy on changing in symptoms in pediatric patients with chronic rhinosinositis

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT2012081810409N3

Enrollment

Registered

2012-09-07

Start date

2011-09-23

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 Rhinosinusitis. Chronic sinusitis, unspecified

Interventions

Intervention 1: adenoidectomy surgery. Intervention 2: adenotonsillectomy surgery.

Treatment - Surgery

Treatment - Drugs

adenoidectomy surgery

adenotonsillectomy surgery

Eligibility

Sex/Gender

All

Age

No minimum to 14 Years

Inclusion criteria

Inclusion criteria: inclusin criteria: children -under the age of 14 years- subjects with chronic sinusitis were recruited from patients referred to otolaryngology clinic,Besat hospital Hamedan University of Medical Science.symptoms and signs of this patient include purulent discharge,facial pain, post nasal purulent discharge,cough,halitosis and bilateral maxillary mucosal thickening in water's view radiography.symptoms and signs of patient did not improved with medical therapy(oral antibiotic & anti allergy for at least 4 weeks). exclusion critera: 1-children with chronic sinusitis with tonsil size and grade have less than 2-tonils occupy less than 25% of their oropharyngeal space - 2-patient with systemic diseases such as diabetes,anemia,immunodificiency,nasal polyposis ,...

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
NasalL Obstruction/Blocage. Timepoint: Before surgery-one month after surgery. Method of measurement: visual analogue scale.;Halitosis. Timepoint: Before surgery-one month after surgery. Method of measurement: visual analogue scale.;Facial pain/pressure. Timepoint: Before surgery-one month after surgery. Method of measurement: visual analogue scale.;Nasal discharge. Timepoint: Before surgery-one month after surgery. Method of measurement: visual analogue scale.;Posterior drange. Timepoint: Before surgery-one month after surgery. Method of measurement: visual analogue scale.;Cough. Timepoint: Before surgery-one month after surgery. Method of measurement: visual analogue scale.;Waters view radiography. Timepoint: Before surgery-one month after surgery. Method of measurement: Questionare.	—

Measure

Time frame

NasalL Obstruction/Blocage. Timepoint: Before surgery-one month after surgery. Method of measurement: visual analogue scale.;Halitosis. Timepoint: Before surgery-one month after surgery. Method of measurement: visual analogue scale.;Facial pain/pressure. Timepoint: Before surgery-one month after surgery. Method of measurement: visual analogue scale.;Nasal discharge. Timepoint: Before surgery-one month after surgery. Method of measurement: visual analogue scale.;Posterior drange. Timepoint: Before surgery-one month after surgery. Method of measurement: visual analogue scale.;Cough. Timepoint: Before surgery-one month after surgery. Method of measurement: visual analogue scale.;Waters view radiography. Timepoint: Before surgery-one month after surgery. Method of measurement: Questionare.

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Mohammad Ahmadi

Hamedan University of Meical Science

M.AHMADI@UMSHA.AC.IR+98 81 1827 9042

Outcome results

None listed

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