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Wound Healing After Endoscopic Sinus Surgery

A

Assiut University

Status

Not yet enrolling

Conditions

Chronic Sinusitis
Nasal Polyps

Treatments

Combination Product: Thymoquinone (0.5%) and Olive oil ointment

Study type

Interventional

Funder types

Other

Identifiers

NCT06070311
endoscopic sinus surgery

Details and patient eligibility

About

This study aims to determine the effect of Thymoquinone (0.5%) and olive oil ointment on Wound healing after Endoscopic sinus surgery.

Full description

Endoscopic sinus surgery (ESS) has become a widely accepted procedure for medically refractory chronic rhino sinusitis and nasal polyps. Over 250,000 endoscopic sinus surgeries are performed yearly in the United States alone, however, postoperative complications and disease recurrence requiring revision surgery are reported in 14% to 24% of patients in long-term follow-up.

There is an increasing interest in interventions and therapies targeted at optimizing outcomes and preventing revision surgery which often depends on good wound healing and less adhesion formation.

The choice of appropriate post-surgical topical treatments is important for healing time and for preventing mucosal complications such as adhesions, crusting formation, and atrophy with secondary bacterial and fungal infections in this light this study aims to determine the effect of thymoquinone and olive oil ointment on wound healing after ESS.

Thymoquinone (TQ) is the most abundant constituent of the volatile oil of Nigella sativa seeds and most properties of Nigella sativa are mainly attributed to TQ. Several pharmacological actions and therapeutic potentials of TQ have been investigated including being antioxidant, anti-inflammatory, antihistaminic, antimicrobial, anti-allergic, anti-fibrotic, and anti-cancer.

Olive oil plays an important role in wound healing process due to its content of phenolic compounds accelerating wound healing through their anti-inflammatory, antioxidant, and antimicrobial properties and their stimulation of angiogenic activities required for granulation tissue formation and wound re-epithelialization.

This Double Blinded Randomized Prospective Comparative study will follow patients with nasal polyposis who are indicated for endoscopic sinus surgery at the Department of Otorhinolaryngology in Assiut University Hospital during the period from the 1st of October 2023 to the 31st of September 2025.

At baseline (before surgery), a full medical history, an otorhinolaryngological examination, and pre-operative screening will be performed to ensure eligibility for the study. The patients will be informed about the surgical procedures, the potential risks of the surgery, and the aim and methodology of the study.

(A) Preoperative:

Full history taking:

  1. Personal History
  2. History of Sino-nasal symptoms e.g., nasal obstruction, nasal discharge, headache, hyposmia, facial congestion, etc.
  3. Other ENT symptoms
  4. General symptoms e.g., asthma, allergy, etc.
  5. Medical history e.g., steroids, antibiotics, anticholinergics, etc.
  6. History of nasal surgery
  7. SNOT 22 questionnaire: To assess preoperative severity of symptoms.

Full medical examination:

  1. General examination

  2. Full ENT examination

  3. Nasal Endoscopy:

    • To evaluate polyp size, site, extent, and consistency.

Investigations:

  1. Routine preoperative investigations: CBC, prothrombin time and concentration
  2. Radiological investigations: Multi-slice CT scan of the nose and paranasal sinuses axial and coronal cuts without contrast and each patient will be scored according to Lund-Mackay CT scoring.

Preparation of the Thymoquinone and Olive oil ointment:

Thymoquinone Oleaginous base ointment containing olive oil will be prepared for intranasal administration. The ointment will be prepared using the fusion method as follows:

Anhydrous lanolin and white soft paraffin will be melted at 70°C and then olive oil will be added with continuous stirring, Thymoquinone will be added to the congealing mixture as it is being cooled and stirred finally, the congealing mixture is left to cool at room temperature tell solidification and sterilized using UV radiation. The final product will be characterized for spreadability, drug content, drug release and stability.

(B) Intraoperative: All cases will be performed under general anaesthesia and the ESS procedure performed by the senior author is that defined by Kennedy.

Immediately after performing the ESS, Thymoquinone and olive oil Ointment will be applied to fill the ethmoidal and different sinuses cavities of one randomly chosen side of the nose, the selected side will be chosen randomly using the following online randomizer tool:

Randomizer | Random Name/Number Picker - AnnaBet.com Then nasal packing with nasal sponge will be done for both sides.

(C) Postoperative: Patients will attend routine follow-up at 1, 2,3,4,8 and 12 weeks after surgery. At these visits, an endoscopic inspection will be performed, and the patients will undergo debridement of the ethmoid cavities when necessary. In addition, endoscopic data regarding the health of the Sino nasal mucosa will be collected. An independent investigator blinded to the side of TQ, and olive oil ointment placement will assess and compare the wound healing in both sides regarding adhesions, crust formation, granulation, infection and score each item using the scoring mentioned below.

Crust formation:

0: No crust formation observed.

  1. Thin and easily removable crusts.
  2. Moderate crust formation, requiring gentle removal.
  3. Thick and adherent crusts, requiring careful and meticulous removal.

Adhesions:

0: No adhesions observed.

  1. Mild adhesions, limited to small areas.
  2. Moderate adhesions, affecting larger areas but without complete obstruction.
  3. Severe adhesions, causing significant obstruction and impaired sinus drainage. 3.Granulation:

0: No granulations observed.

  1. Mild granulation tissue, with minimal vascularity and minimal elevation.
  2. Moderate granulation tissue, with moderate vascularity and noticeable elevation.
  3. Severe granulation tissue, with marked vascularity and significant elevation. 4.Infection:

0: No signs or symptoms of infection observed.

  1. Mild infection, mucopurulent discharge limited to small area of the ethmoidal cavity.
  2. Moderate infection, mucopurulent discharge filling one sinus.
  3. Severe infection, mucopurulent discharge filling more than one sinus.

Participants will take the SNOT-22 questionnaire after the operation at the follow up visits to evaluate sino nasal symptoms.

Enrollment

50 estimated patients

Sex

All

Ages

18 to 75 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • All patients who will be clinically diagnosed and radiologically confirmed cases with bilateral nasal polyposis indicated for Endoscopic sinus surgery.

Exclusion criteria

  1. Unfit patient for surgery

  2. Pregnant and lactating women.

  3. Patients unwilling to participate.

  4. Patients who have unilateral disease.

  5. Patients with a history of the following underlying medical conditions, which are associated with an increased rate of revision surgery, will be excluded from the study:

    1. Aspirin intolerance
    2. Asthma
    3. Mucociliary disorder
    4. Immunocompromised status.
  6. Patients with known allergic reactions to Thymoquinone or olive oil.

  7. Injury of the orbit with any tear in the periorbital area.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

50 participants in 2 patient groups

Thymoquinone (0.5%) and Olive oil ointment
Active Comparator group
Description:
thymoquinone (0.5%) and olive oil ointment will be applied to fill the ethmoidal and different sinuses cavities of one randomly chosen side of the nose.
Treatment:
Combination Product: Thymoquinone (0.5%) and Olive oil ointment
No intervention
No Intervention group
Description:
no intervention

Trial contacts and locations

0

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Central trial contact

Mohamed Mostafa Osman, Professor; Ahmed Gamal Sholkamy, Doctor

Data sourced from clinicaltrials.gov

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