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Faringomoss Effectiveness in Inhibiting Acute Throat Pain and Discomfort

NCT02894372 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 96

Last updated 2017-03-13

No results posted yet for this study

Summary

The purpose of the study was to assess the effectiveness of Faringomoss in reducing the throat discomfort and pain in patients with acute throat diseases and postoperative patients after throat surgeries.

Conditions

  • Spraying Behavior
  • Mouth Diseases
  • Throat Diseases
  • Throat Pain

Interventions

DEVICE

Oral spray 1

Research participants got topical oral spray immediately after surgery (hospital patients) and from the first doctor visit with pharyngeal disease (clinic outpatients).

DEVICE

Oral spray 2

Research participants got topical oral spray immediately after surgery (hospital patients) and from the first doctor visit with pharyngeal disease (clinic outpatients).

Sponsors & Collaborators

  • Klaipėda University

    collaborator OTHER

  • Vita Longa Clinic

    collaborator UNKNOWN

  • Lithuanian University of Health Sciences

    lead OTHER

Principal Investigators

  • Nora Siupsinskiene, Professor · Hospital of Lithuanian University of Health Sciences, Otorhinolaryngology department

  • Nora Siupsinskiene, Professor · Klaipėda University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
6 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-01-31
Primary Completion
2016-11-01
Completion
2016-12-30

Countries

  • Lithuania

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02894372 on ClinicalTrials.gov