Clinical Outcomes and Patient Satisfaction With Velnez Versus Nasopore in Nasal Surgery
NCT: NCT07560254 · COMPLETED
Brief Summary
This clinical trial evaluated two absorbable nasal packing materials - VELNEZ and NASOPORE - in adult patients (18-70 years) who underwent nasal surgery, including septoplasty, FESS, or turbinoplasty. The study addressed two core questions: whether VELNEZ offered superior haemorrhage control and faster biodegradation, and whether it reduced postoperative pain, fibrosis, adhesion, and discomfort compared to NASOPORE. Participants were randomised to receive either packing material following surgery. They were monitored on the day of surgery for haemostasis and device performance, then followed up with clinical and endoscopic assessments - including pain scoring and adverse event tracking - through Day 90.
Frequently Asked Questions
What is Clinical Outcomes and Patient Satisfaction With Velnez Versus Nasopore in Nasal Surgery?
Clinical Outcomes and Patient Satisfaction With Velnez Versus Nasopore in Nasal Surgery is a clinical trial registered under NCT07560254. Current status: COMPLETED.
What is the status of NCT07560254?
The current status of NCT07560254 (Clinical Outcomes and Patient Satisfaction With Velnez Versus Nasopore in Nasal Surgery) is: COMPLETED.
When did Clinical Outcomes and Patient Satisfaction With Velnez Versus Nasopore in Nasal Surgery start?
Clinical Outcomes and Patient Satisfaction With Velnez Versus Nasopore in Nasal Surgery started on 2024-09-11.
Official Source
View on ClinicalTrials.gov →Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.