Patient Guide: Study to Evaluate the Efficacy and Safety of Different Doses of Graminidin With Anesthetic, a Metered Dose Topical Spray, in the Treatment of Acute Infectious and Inflammatory Pharyngeal Diseases Compared With Drug Septolete Total, Lozenges

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 12 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT06843018
Status: 🟢 Enrolling Now
Condition: Pharyngitis, Nasopharyngitis, Pharyngeal Diseases
Phase: PHASE2

Where You Can Participate

This study is available at 12 locations across the country.

Top locations include:
  • • Engels,
  • • Kaliningrad,
  • • Moscow,
  • • And 9 more locations

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Study to Evaluate the Efficacy and Safety of Different Doses of Graminidin With Anesthetic, a Metered Dose Topical Spray, in the Treatment of Acute Infectious and Inflammatory Pharyngeal Diseases Compared With Drug Septolete Total, Lozenges - Join Clinical Trial NCTNCT06843018

How to Join This Clinical Trial - NCTNCT06843018

Learn how to participate in this PHASE2 trial studying an investigational therapy for Pharyngitis, Nasopharyngitis, Pharyngeal Diseases. This study is currently enrolling participants.

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with Pharyngitis, Nasopharyngitis, Pharyngeal Diseases. Eligibility requirements include specific age ranges, health status, and medical history. Contact the study team to learn if you qualify.

Condition Being Studied
Pharyngitis, Nasopharyngitis, Pharyngeal Diseases
Treatment Being Tested
Investigational treatment
Study Phase
PHASE2 - Safety and effectiveness study
Enrollment Status
Currently enrolling participants
Study Identifier
NCTNCT06843018 - ClinicalTrials.gov Identifier
Sponsored By
Study sponsor

What to Expect as a Participant

Participating in this clinical trial involves:

  • Initial screening to determine eligibility
  • Regular study visits and health assessments
  • Receiving the study treatment or placebo
  • Medical monitoring and follow-up care
  • Contributing to medical research that may help others
  • Potential access to new treatments before they're widely available

Clinical Trial Benefits and Compensation

Participants in this clinical research study may receive:

  • Close medical monitoring by healthcare professionals
  • Access to potential new treatments
  • Compensation for time and travel (varies by study)
  • No-cost study-related medical care
  • The opportunity to help advance medical knowledge

Where Is This Clinical Trial Located?

This study is enrolling participants at 12 locations. Find a study site near you:

Clinical Research Site

Engels, 413116 - Russian Federation

Status: RECRUITING

Clinical Research Site

Kaliningrad, - Russian Federation

Status: RECRUITING

Clinical Research Site

Moscow, 119571 - Russian Federation

Status: RECRUITING

Clinical Research Site

Perm, 614070 - Russian Federation

Status: RECRUITING

Clinical Research Site

Saint Petersburg, 194156 - Russian Federation

Status: RECRUITING

Clinical Research Site

Saint Petersburg, 194358 - Russian Federation

Status: RECRUITING

Clinical Research Site

Saint Petersburg, 196158 - Russian Federation

Status: RECRUITING

Clinical Research Site

Saint Petersburg, 199406 - Russian Federation

Status: RECRUITING

Clinical Research Site

Saint Petersburg, - Russian Federation

Status: RECRUITING

Clinical Research Site

Saratov, - Russian Federation

Status: RECRUITING

And 2 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this PHASE2 clinical trial for Pharyngitis, Nasopharyngitis, Pharyngeal Diseases:

  1. Review the eligibility criteria with your healthcare provider
  2. Contact the study team for a pre-screening interview
  3. Schedule an in-person screening visit if eligible
  4. Review and sign the informed consent form
  5. Begin participation in the clinical trial

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