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Role of Topical Decongestant to Relieve Early Postoperative Symptoms Following Inferior Turbinoplasty: A prospective randomized controlled trial

Role of Topical Decongestant to Relieve Early Postoperative Symptoms Following Inferior Turbinoplasty: A prospective randomized controlled trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
TCTR
Registry ID
TCTR20210622004
Enrollment
30
Registered
2021-06-22
Start date
2021-06-29
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Patients who were suffering from chronic nasal obstruction secondary to inferior turbinate hypertrophy who failed at least 3-month medication therapy to control nasal obstructive symptom. topical decongestant, turbinoplasty, oxymetazoline, postoperative care

Interventions

Patients receive physiologic saline nasal irrigation with 125-mL, 4times daily and oxymetazoline hydrochloride 0.05% nasal spray, 1puff to each nostril 3 times a day for 7 days, post-operative tubinec
Active Comparator Drug,Placebo Comparator Drug
Oxymetazoline nasal spray group,Control group

Sponsors

None listed

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age>18years 2. Patients who were suffering from chronic nasal obstruction secondary to inferior turbinate hypertrophy who failed at least 3-month medication therapy to control nasal obstructive symptom and plan to go on the turbinate reduction procedure are enrolled into the study.

Exclusion criteria

Exclusion criteria: 1. Any other inflammatory or infectious diseases or tumor of sinonasal cavities i.e. Wegener's disease, cystic fibrosis and lymphoma 2. Clinical or radiologic or endoscopic evidence of rhinosinusitis with or without nasal polyp 3. Clinical or radiologic or endoscopic evidence of severe septal deviation without correction 4. Rhinitis medicamentosa 5. Long term vasoconstrictor drug use 6. Disorder of nasal valve 7. Pregnancy 8. The patients who refuse to enroll the study

Design outcomes

Primary

MeasureTime frame
nasal obstructive symptom preoperative, postoperative day1-day7(mean VAS score), at 2 week and at 1 month Nasal Obstruction Symptom Evaluation (NOSE),severity of nasal obstruction, frequency of nasal obstruction, rhinorrhea, sneezing, itchy nose, headache, hyposmia, snoring preoperative, postoperative day 1-day7 (mean VAS score), 2 week and at 1 month Visual analog scale (VAS score)

Secondary

MeasureTime frame
Crusting postoperative 1 week, 2 week and at 1 month Crusting score,bleeding severity postoperative day 1-day 7(mean score) bleeding severity grading ,Inferior turbinate size preoperative, postoperative 1 week, 2 week and 1 month 4-point ordinal scale,Pain postoperative day 1 -day7 (mean score) Pain score,nasal airway resistance preoperative, postoperative 1 week and 1 month Anterior rhinomanometry,Side effects of decongestant preoperative, postoperative 1 week Heart rate and blood, Topical effects such as burning, stinging, irritation and dryness in the nose will be recorded pressure,Mucociliary function preoperative and postoperative 1 month saccharin test

Countries

Thailand

Contacts

Public ContactJidapa Tragoonrungsea

Faculty of Medicine Ramathibodi Hospital, Mahidol University

janjy.t@gmail.com0841134459

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026