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Recruiting NCT07745127

Comparative Study - Transseptal Suture Technique Verses Anterior Nasal Packing After Septoplasty

No phase Interventional Deviated Nasal Septum Postoperative Nasal Pain Postoperative Nasal Bleeding

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Trans-septal suture technique, Anterior nasal packing.
Who it may be relevant to
Registry conditions: Deviated Nasal Septum, Postoperative Nasal Pain, Postoperative Nasal Bleeding. Basic parameters: 18 years — 50 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Pakistan
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Trans Septal Suture Technique Verses Anterior Nasal Packing After Septoplasty - A Comparative Study

Overview

The goal of this clinical trial is to see the outcomes of the two techniques used after septoplasty in terms of postoperative nasal pain and nasal bleeding in the patients with deviated nasal septum of 18 to 50 years of age presented in a tertiary care hospital. The main questions it aims to answer are: 1. any significant difference between the two techniques in terms of post operative nasal pain? 2. any significant difference between the two techniques in terms of post operative nasal bleeding? Researchers will be comparing the outcomes of these two techniques while participants already admitted in ward will be examined on 1st postoperative day.

Interventions

  • Procedure Trans-septal suture technique
    Trans-septal suture technique in septoplasty
  • Procedure Anterior nasal packing
    ANP

Primary outcome measures

  • Post operative Nasal Pain [Time frame: 24 hours after surgery on first post operative day]
Secondary outcome measures (1)
  • Post operative nasal hemorrhage [Time frame: 24 hours after surgery on first post operative day]

Eligibility criteria

Inclusion criteria

  • symptomatic deviated nasal septum
  • 18-50 years of age
  • both male and female genders

Exclusion criteria

  • history of previous nasal surgery
  • presence of chronic rhinosinusitis with or without nasal polyposis
  • pregnant females
  • immunocompromised patients
  • patients with pulmonary and/or cardiovascular disorders
  • patients those who received steroidal or anticoagulant therapy within last 30 days.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Double blind
Primary purpose
Treatment

Study locations

Pakistan · 1 center
  • Pakistan Institute of Medical Sciences (PIMS), Islamabad. — Islamabad

Publications

  • Wang D, Liu T, Liao C, Tang G, Tian T, Tian L. Is nasal septal suturing an alternative technique to nasal packing?: A protocol for systematic review and meta-analysis. Medicine (Baltimore). 2020 Dec 11;99(50):e23535. doi: 10.1097/MD.0000000000023535. PMID 33327302
  • Ivanova PP, Iliev G. Nasal Packing in Septal Surgery: A Narrative Review. Cureus. 2023 Mar 21;15(3):e36488. doi: 10.7759/cureus.36488. eCollection 2023 Mar. PMID 37090361
  • Alsaggaf ZH, Almadfaa AO, Marouf AA, Alfawaz KS, Niyazi RA, Ibrahim NK, Ajlan AM. Sinusitis and its association with deviated nasal septum at a tertiary hospital: A retrospective study. J Taibah Univ Med Sci. 2022 Jun 18;17(6):1065-1069. doi: 10.1016/j.jtumed.2022.06.001. eCollection 2022 Dec. PMID 36212586
  • Alghamdi FS, Albogami D, Alsurayhi AS, Alshibely AY, Alkaabi TH, Alqurashi LM, Alahdal AA, Saber AA, Almansouri OS. Nasal Septal Deviation: A Comprehensive Narrative Review. Cureus. 2022 Nov 10;14(11):e31317. doi: 10.7759/cureus.31317. eCollection 2022 Nov. PMID 36514566

Identifiers

NCT: NCT07745127 · No.F.1-1/2015/ERB/SZABMU/1428

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗