Outcomes of PRF on Septoplasty in Patient With Nasal Septal Deviation

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
AgeUp to 65
SponsorKafrelsheikh University

About this trial

The aim of this study is to assess the effectiveness of Platelet-Rich Fibrin (PRF) in improving postoperative healing, reducing complications, and enhancing functional outcomes in patients undergoing septoplasty

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Adults aged 18-65 years undergoing septoplasty. Presence of cartilage deviated nasal septum requiring repair. No contraindications to PRF therapy.

Disqualifiers

History of coagulopathy or anticoagulant therapy. Active infection or systemic disease. Known hypersensitivity to PRF components. Previous nasal surgery Autoimmune or systemic inflammatory disease

Trial design

Design model

Parallel

Treatments tested in this trial

  • Effect of Platelet Rich Fibrin on Septoplasty

    Other intervention

    it is a randomized trial of usage of platelet rich fibrin in septoplasty

Treatment groups

100 Participants
are divided into 2 treatment groups
Group A: platelet rich fibrinActive comparator 1 intervention
Group B: control groupActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Effect of submucoperichondrial application of platelet rich fibrin on healing of nasal septum mucosa after septoplasty

Mucosal Healing will be assessed by visual nasal endscope

Time frame
postoperative at 1st week , 1st month , 3rd month

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

This trial is not recruiting at the moment. You can still explore other options: