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Buparid/PARI SINUS Versus Budes® Nasal Spray in the Therapy of Chronic Rhinosinusitis With Polyposis Nasi

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT01946711
Recruitment Status : Unknown
Verified April 2018 by Pari Pharma GmbH.
Recruitment status was:  Recruiting
First Posted : September 20, 2013
Last Update Posted : April 26, 2018
Information provided by (Responsible Party):
Pari Pharma GmbH

Brief Summary:
The study should create data for the selection of a clinically relevant primary endpoint to assess the efficacy and safety of Buparid/PARI SINUS as compared to Budes Nasal Spray in the therapy of chronic rhinosinusitis (CRS) with polyposis nasi in adult patients. Ideally, the selected parameter should allow a correlation between an objective methodology and the clinical outcome of the study patients.

Condition or disease Intervention/treatment Phase
Rhinosinusitis Chronic Polyposis Drug: Budesonide Phase 3

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 20 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: A Pilot Study to Investigate the Efficacy and Safety of Buparid/PARI SINUS Versus Budes® Nasal Spray in the Therapy of Chronic Rhinosinusitis (CRS) With Polyposis Nasi in Adult Patients
Study Start Date : April 2014
Estimated Primary Completion Date : December 2018
Estimated Study Completion Date : May 2019

Resource links provided by the National Library of Medicine

Drug Information available for: Budesonide

Arm Intervention/treatment
Experimental: Buparid; Treatment A
Buparid 1 mg budesonide/2 ml nebuliser solution
Drug: Budesonide

Active Comparator: Budes; Treatment B
Budes® Nasal Spray 50 µg budesonide/pump
Drug: Budesonide
Nasal spray

Primary Outcome Measures :
  1. Change of inflammation of the nasal mucosa and paranasal sinus [ Time Frame: Change from Baseline at Week 8 ]

    Magnetic Resonance Imaging

    • Thickness of mucosa
    • Lund-Mackay-Score

Secondary Outcome Measures :
  1. Safety assessment [ Time Frame: 26 weeks ]
    Treatment-emergent adverse events (AEs)

Other Outcome Measures:
  1. Health-specific quality of life [ Time Frame: 26 weeks ]
    SNOT 22 (Sino-Nasal Outcome Test 22)

  2. Nasal obstruction [ Time Frame: 8 weeks ]

  3. Expansion of polyposis nasi [ Time Frame: Week 0 and Week 8 ]
    Endoscopy (classification according to Rasp et al. 2000)

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  • Patient with confirmed diagnosis of chronic rhinosinusitis (CRS) with polyposis nasi grade I-III
  • Patient with a PNIF of > 7 l/min separated for left and right side of the nose
  • Patient's written informed consent
  • Male or female,>= 18 years of age
  • Patient is able to undergo nasal therapy without restrictions
  • Capable of understanding the purpose and risk of the clinical trial
  • Female patients with childbearing potential must have a negative urine pregnancy test prior to first IMP administration
  • Patient has completed correctly the diary during the Wash-in Phase

Exclusion Criteria:

  • Patients with cystic fibrosis
  • Patients with polyposis nasi grade IV
  • Patients with prior sinonasal surgery (exemption: polypectomy)
  • Patients with primary ciliaritis
  • Pregnant or breastfeeding women
  • Patients with suspected active upper airway infection
  • Receipt of an investigational drug as part of a clinical trial within 4 weeks prior to first administration of IMP
  • Drug or alcohol abuse
  • End-stage malignancies
  • Known hypersensitivity to Budesonide
  • Patients with oral steroid therapy within the last 4 weeks
  • Patients with frequent epistaxis (> 2 per month)

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its identifier (NCT number): NCT01946711

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Contact: Stefanie Prante +49 89 742846 ext 830

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University Göttingen Completed
Göttingen, Germany, 37075
UNIVERSITÄTSMEDIZIN der Johannes Gutenberg-Universität Mainz Recruiting
Mainz, Germany, 55131
Contact: Sven Becker, MD    +49 (0) 6131 17 ext 2099   
Principal Investigator: Sven Becker, MD         
University LMU Munich Recruiting
Munich, Germany, 81377
Contact: Bernhard Weiss, MD    +49 89 4400 ext 73889   
Principal Investigator: Bernhard Weiss, MD         
HNO-Zentrum Mangfall-Inn Recruiting
Rosenheim, Germany, 83022
Contact: Mareike Haack, MD    +49 8031-12425   
Principal Investigator: Mareike Haack, MD         
Sponsors and Collaborators
Pari Pharma GmbH
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Principal Investigator: Sven Becker, MD Johannes Gutenberg University Mainz
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Responsible Party: Pari Pharma GmbH Identifier: NCT01946711    
Other Study ID Numbers: 12082.101
First Posted: September 20, 2013    Key Record Dates
Last Update Posted: April 26, 2018
Last Verified: April 2018
Keywords provided by Pari Pharma GmbH:
Additional relevant MeSH terms:
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Colorectal Neoplasms
Nasopharyngeal Neoplasms
Paranasal Sinus Diseases
Nose Diseases
Respiratory Tract Diseases
Respiratory Tract Infections
Otorhinolaryngologic Diseases
Intestinal Neoplasms
Gastrointestinal Neoplasms
Digestive System Neoplasms
Neoplasms by Site
Digestive System Diseases
Gastrointestinal Diseases
Colonic Diseases
Intestinal Diseases
Rectal Diseases
Pharyngeal Neoplasms
Otorhinolaryngologic Neoplasms
Head and Neck Neoplasms
Nasopharyngeal Diseases
Pharyngeal Diseases
Stomatognathic Diseases
Anti-Inflammatory Agents
Bronchodilator Agents
Autonomic Agents
Peripheral Nervous System Agents
Physiological Effects of Drugs