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NCT Number: NCT07635459

Thermosensitive Gel Nasal Spray With Exosomes, Azelastine, and Interferon for Acute Phase of Chronic Sinusitis

This study tests a new nasal spray for adults (18-65 years) with chronic sinusitis experiencing an acute phase. The spray contains a temperature-sensitive gel that turns into a soft gel inside the nose to slowly release three active ingredients: stem cell exosomes (to repair nasal lining), azelastine (an antihistamine and anti-inflammatory drug), and interferon alpha-2b (an antiviral agent). The study aims to evaluate safety and see if the spray can reduce symptoms, fight viruses, and improve quality of life. Participants will be randomly assigned to one of three groups: triple spray, dual spray (without exosomes), or placebo (gel only). Treatment is twice daily for 4 weeks, with follow-up visits up to day 90.

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Early Phase 1

About this study

This exploratory, single-centre, randomised, double-blind, placebo-controlled study enrolls 108 participants (allowing 20% dropout) in a 1:1:1 ratio. Group A receives thermosensitive gel + exosomes (1×10^10 particles/mL) + azelastine (0.1%) + interferon α-2b (1×10^5 IU/mL). Group B receives gel + azelastine + interferon (without exosomes). Group C receives blank gel. The gel matrix (Poloxamer 407 18% + chitosan hydrochloride 0.5%) is liquid at room temperature and gels at nasal temperature (33-35°C). Treatment duration is 28 days (twice daily, 2 sprays per nostril). Single-spray doses: exosomes 2×10^9 particles, azelastine 0.2 mg, interferon 2000 IU. Follow-up at day 42 and day 90. Primary outcome: safety (adverse events, CTCAE v5.0). Secondary outcomes: Lund-Kennedy score, SNOT-22, VAS, response rate, SF-36. Exploratory: viral clearance, inflammatory cytokines, bacterial load, mucosal barrier markers. The study is conducted at The First Affiliated Hospital of Xinxiang Medical College. Ethics approval obtained. Results will be published.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age 18 to 65 years, both genders
  • Diagnosis of chronic rhinosinusitis according to Chinese guidelines (2018) or EPOS 2020, duration >12 weeks
  • Lund-Kennedy endoscopic score ≥4
  • SNOT-22 score ≥30
  • Nasal symptoms stable in past month, or acute flare-ups not requiring systemic antibiotics/steroids
  • Voluntary signed informed consent

Exclusion criteria

  • Sinus surgery within past 6 months or anatomical abnormalities requiring reoperation
  • Allergic fungal rhinosinusitis, odontogenic rhinosinusitis, or nasal polyps
  • Primary ciliary dyskinesia, cystic fibrosis, or severe immunodeficiency
  • Use of systemic glucocorticoids, immunosuppressants, or antibiotics within past 4 weeks
  • Use of intranasal glucocorticoids, antihistamines, or leukotriene receptor antagonists within past 2 weeks
  • Hypersensitivity to poloxamer, chitosan, azelastine, or interferon
  • Pregnant, breastfeeding, or planning to become pregnant
  • Uncontrolled severe systemic diseases (diabetes, hypertension, autoimmune diseases)
  • Malignancy within past 5 years
  • Participation in other clinical trials

Treatment and study plan

Exosomes, Azelastine, and Interferon alpha-2b

Drug

Thermosensitive gel nasal spray containing hUC-MSC-Exos (1×10^10 particles/mL), azelastine hydrochloride 0.1%, and interferon α-2b 1×10^5 IU/mL.

Other names: Triple combination spray

Azelastine and Interferon alpha-2b

Drug

Thermosensitive gel nasal spray containing azelastine hydrochloride 0.1% and interferon α-2b 1×10^5 IU/mL.

Other names: Dual combination spray

Placebo Gel Matrix

Drug

Thermosensitive gel matrix (Poloxamer 407 18% + chitosan hydrochloride 0.5% in PBS) only.

Other names: Blank thermosensitive gel

Primary outcomes

  1. Number of Participants with Treatment-Related Adverse Events

    Time frame: From baseline up to day 90 (long-term follow-up)

    Local adverse events (epistaxis, nasal irritation, burning sensation, dryness, ulceration), systemic adverse events (drowsiness, fatigue, headache, nausea, allergic reactions), taste abnormalities (bitter taste), and changes in laboratory parameters (CBC, ALT/AST, Cr/BUN) graded by CTCAE v5.0.

Secondary outcomes

  1. Change in Lund-Kennedy Endoscopic Score

    Time frame: Baseline, Day 29, and Day 42

    Lund-Kennedy Endoscopic Score. Minimum value 0 (normal), maximum value 20 (most severe inflammation). Higher scores mean a worse outcome. This scale assesses polyps, oedema, discharge, scarring, and crusting.

  2. Change in SNOT-22 Score

    Time frame: Baseline, Day 29, Day 42, and Day 90

    Sino-Nasal Outcome Test-22 (SNOT-22) Score. Minimum value 0 (no symptoms), maximum value 110 (worst possible symptoms). Higher scores mean a worse outcome.

  3. Change in VAS Symptom Score (nasal congestion, rhinorrhoea, facial pressure, smell loss)

    Time frame: Daily during treatment (Days 1-28) and follow-up up to Day 90

    Visual Analog Scale (VAS) for nasal symptoms. Minimum 0 (no distress), maximum 10 (worst imaginable distress). Higher scores mean a worse outcome.

  4. Response Rate (SNOT-22 improvement ≥15 points or ≥50%)

    Time frame: Day 29

  5. Change in Quality of Life (SF-36)

    Time frame: Baseline and Day 29

    36-Item Short Form Health Survey (SF-36). Scores range from 0 to 100. Higher scores indicate better quality of life.

Study contacts

Contact information is provided by the study sponsor or research team.

Wenfa Yu, MD, PhD

CONTACT

[email protected]

86+15516510606

Wenjie Ren, MD, PhD

CONTACT

[email protected]

86+13837310327

Sponsors and collaborators

Lead sponsor

The First Affiliated Hospital of Xinxiang Medical College

Other

Registry information

Official study title

A Single-Centre, Randomised, Double-Blind, Placebo-Controlled Exploratory Clinical Study of a Thermosensitive Gel Nasal Spray Containing Umbilical Cord Mesenchymal Stem Cell-Derived Exosomes, Azelastine and Recombinant Human Interferon α-2b for the Treatment of Chronic Rhinosinusitis (Acute Phase)

Acronym: CRS

Important dates

Study start
2026
Primary completion
2027
Study completion
2027
First posted
Jun 9, 2026
Registry last updated
Jun 9, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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