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Recruiting Phase 2 NCT07340411

NCT07340411 Effect of Chinese Herbal Medicine Nasal Irrigation on the Postoperative Care of Chronic Rhinosinusitis

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Clinical Trial Summary
NCT ID NCT07340411
Status Recruiting
Phase Phase 2
Sponsor Taichung Veterans General Hospital
Condition Chronic Rhinosinusitis
Study Type INTERVENTIONAL
Enrollment 80 participants
Start Date 2023-07-05
Primary Completion 2026-03-01

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age 90 Years
Study Type INTERVENTIONAL
Interventions
Chinese herbal medicine PowderSalt Powder

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

In Phase 2, researchers evaluate early signs of effectiveness. You may be randomized to receive the active treatment or a comparator. Monitoring continues closely.

This trial targets 80 participants in total. It began in 2023-07-05 with a primary completion date of 2026-03-01.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

Investigators tried to evaluate the efficacy and safety of Chinese herbal medicine nasal irrigation as an adjuvant therapy after FESS.

Eligibility Criteria

Inclusion Criteria: * 1\. Patients with chronic rhinosinusitis who failed medical treatment 2.Patients underwent bilateral primary functional endoscopic sinus surgery. Exclusion Criteria: * 1\. Patients with a history of immunodeficiency 2.Patients with a history of sinus surgery 3.Patients who receiving antibiotic treatment within a week before functional endoscopic sinus surgery 4.Patients with a pathological diagnosis of fungal sinusitis 5.Patients with a pathological diagnosis of sinonasal tumor

Contact & Investigator

Central Contact

Rong-San Jiang, MD, PhD

✉ rsjiang@vghtc.gov.tw

📞 886-4-23592525

Principal Investigator

Rong-San Jiang, MD, PhD

PRINCIPAL INVESTIGATOR

Taichung Veterans General Hospital

Frequently Asked Questions

Who can join the NCT07340411 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, up to 90 Years, studying Chronic Rhinosinusitis. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

What phase is the NCT07340411 trial and what does that mean for participants?

Phase 2 trials evaluate whether the treatment shows signs of effectiveness while continuing to monitor safety. More participants are enrolled than in Phase 1 to help refine the treatment protocol.

Is NCT07340411 currently recruiting?

Yes, NCT07340411 is actively recruiting participants. Contact the research team at rsjiang@vghtc.gov.tw for enrollment information.

Where is the NCT07340411 trial being conducted?

This trial is being conducted at Taichung, Taiwan.

Who is sponsoring the NCT07340411 clinical trial?

NCT07340411 is sponsored by Taichung Veterans General Hospital. The principal investigator is Rong-San Jiang, MD, PhD at Taichung Veterans General Hospital. The trial plans to enroll 80 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: July 2026  ·  Data Methodology