paranasal sinus accessibility of large volume saline in postoperative FESS patient by intranasal instillation in various head positions

Status

Active, not recruiting

Phases

Phase 1

Study type

Interventional

Source

TCTR

Registry ID

TCTR20160128001

Enrollment

Unknown

Registered

2016-01-28

Start date

2016-01-28

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

paranasal sinus accessibility when instillation of normal saline in various head positions paranasal sinus accessibility&#44

Interventions

vertex to floor position when instillation normal saline,mygind when instillation normal saline,ragan when instillation normal saline

Experimental Other,Experimental Other,Experimental Other

vertex to floor,mygind,ragan

Eligibility

Sex/Gender

All

Age

18 Years to 0 Years

Inclusion criteria

Inclusion criteria: 1. patient age >= 18 years 2. postoperative FESS in Srinagarind hostpital in 4 weeks 3. opening of all sinus adequately 4. be able to cooperative

Exclusion criteria

Exclusion criteria: 1. DNS which not have correct 2. tumor in paranasal sinus or nasal cavity 3. use to skull base surgry before 4. fibrous that obstruct or inadequate opening of sinus 5. allergy cintrast media or seafood 6. pregnancy 7. acute sinusitis 8. cleft lip and not yet surgery for repaire 9. allergic xylocaine or oxymetazoline

Design outcomes

Primary

Measure	Time frame
paranasal sinus accessibility 2-4 weeks pilot study, mix contrast media and normal saline for instillation before evaluated by CT paranasal	—

Secondary

Measure	Time frame
- - -	—

Countries

thailand

Contacts

Public Contactpanwad luangprasert

ENT department

go2goldgoal@hotmail.com0827493818

Outcome results

None listed

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