CClinicalTrials.gg
Not yet recruitingNCT06996106Updated May 30, 2025

Outcomes of PRF on Septoplasty in Patient With Nasal Septal Deviation

An interventional study of Effect of Platelet Rich Fibrin on Septoplasty in Nasal Septum; Deviation and Nasal Septal Srur, sponsored by Kafrelsheikh University. Not yet recruiting. Open to participants aged Up to 65 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2025-05-30.

Sponsored by Kafrelsheikh University · Not applicable, Interventional, and Other

From the registry’s dates

  • Primary completion was expected by Jan 2026, 9 months ago, but the record still lists the study as not yet recruiting.
Phase
Not applicable
Study type
Interventional
Enrollment
100
Allocation
Not applicable
Ages
Up to 65 Years
Sex
All
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Study summary

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

Read the detailed description

Septoplasty is a routine surgical intervention to correct nasal septal deviation, a major cause of nasal obstruction and chronic sinusitis. Despite advancements, postoperative complications-such as mucosal injury, synechiae, septal perforation, and hematoma-continue to impact outcomes and patient satisfaction.

Platelet-rich fibrin (PRF), first described by Choukroun et al., represents an autologous biomaterial rich in growth factors like PDGF, TGF-β, VEGF, and IGF-1, known to accelerate wound healing and tissue regeneration. Unlike platelet-rich plasma (PRP), PRF is easier to prepare, does not require anticoagulants, and forms a fibrin matrix conducive to sustained release of cytokines.

Several studies across disciplines-oral surgery, dermatology, orthopedics-support the regenerative potential of PRF. In nasal surgery, the delicate mucosal environment could benefit significantly from enhanced healing facilitated by PRF.

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Conditions studied

  • Nasal Septum; Deviation
  • Nasal Septal Srur
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In context

Lead sponsor

Kafrelsheikh University is the lead sponsor of 285 studies on the registry; 110 are open to participants now.

Of its 9 completed or terminated interventional studies of FDA-regulated products, 0 (0%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
Up to 65 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

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

Exclusion criteria

Exclusion Criteria:

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

Phase
Not applicable
Primary purpose
Other
Allocation
Not applicable
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
100 participants (estimated)

Study arms

  • Active comparator
    platelet rich fibrin

    usage of platelet rich fibrin in this arm underging setoplasty

    Other: Effect of Platelet Rich Fibrin on Septoplasty

  • Active comparator
    control group

    traditional septoplasty

    Other: Effect of Platelet Rich Fibrin on Septoplasty

Interventions

  • OtherEffect of Platelet Rich Fibrin on Septoplasty

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

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What researchers measure

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

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Study locations

No study locations are listed for this record.

08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 30, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT06996106
Lead sponsor
Kafrelsheikh University
Responsible party
Ahmed Ibrahim Abdallah Abdel wahd Abo Hussein (ahmed ibrahim, Kafrelsheikh University) — Principal investigator
First posted
May 30, 2025
Start date
Jun 2025 (estimated)
Primary completion
Jan 1, 2026 (estimated)
Completion
Feb 1, 2026 (estimated)
Last update
May 30, 2025

Study contacts

‪Ahmed ibrahim‬, M.B.B. Ch, Otorhinolary
Contact
ai731540@gmail.com
0201014848903

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in May 2025. You cannot join it, but the record below documents what was studied.

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