Comparative Efficacy of the Suppository Versus Guaiacol Suppository Versus Guaifenesin Syrup in Pediatric Patients With Cough Due the Infectious Origin
NCT01119534 · Status: UNKNOWN · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 270
Last updated 2011-01-28
Summary
It is believed that the suppository consisting of guaiacol, menthol, camphor and eucalyptol, by their pharmacological properties already established for each component, has the ability to reduce the signs and symptoms related to upper respiratory infections in a manner equivalent (not inferior) to medicine used as a comparator in this study and higher than the suppository containing only guaiacol concentration of 12.5 mg.
Conditions
Interventions
- DRUG
-
Guaiacol, eucalyptol, menthol and camphor suppository
2 times per day
- DRUG
-
guaiacol suppository
2 times per day
- DRUG
-
Guaifenesin syrup
4.19 mL - 4 in 4 hours
Sponsors & Collaborators
-
Azidus Brasil
lead INDUSTRY
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 2 Years
- Max Age
- 6 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2011-05-31
- Primary Completion
- 2011-10-31
- Completion
- 2011-12-31
Countries
- Brazil
Study Locations
More Related Trials
-
A Real-world Evidence Study of BNT162b2 mRNA Covid-19 Vaccine Among Children in Brazil
NCT05403307 ·Status: COMPLETED
-
A Study to Evaluate Safety and Effectiveness of mRNA-1273 COVID-19 Vaccine in Healthy Children Between 6 Months of Age and Less Than 12 Years of Age
NCT04796896 ·Status: COMPLETED ·Phase: PHASE2/PHASE3
-
Efficacy, Safety, and Immunogenicity of V260 in Healthy Chinese Infants (V260-024)
NCT02062385 ·Status: COMPLETED ·Phase: PHASE3
-
Efficacy and Safety of Gefapixant (MK-7264) in Women With Chronic Cough and Stress Urinary Incontinence (MK-7264-042)
NCT04193176 ·Status: COMPLETED ·Phase: PHASE3
-
Dose Confirmation Efficacy Study (V260-007)
NCT00092443 ·Status: COMPLETED ·Phase: PHASE3
-
Improving Vaccine Counseling Skills Among Residents Using Educational Modules and Standardized Patient Encounters
NCT06074237 ·Status: COMPLETED ·Phase: NA
-
A Phase 1/2/3 Study to Evaluate the Safety, Tolerability, and Immunogenicity of an RNA Vaccine Candidate Against COVID-19 in Healthy Children
NCT04816643 ·Status: COMPLETED ·Phase: PHASE2/PHASE3
-
A Study of the Immunogenicity, Tolerability, and Safety of a New Formulation of RotaTeq™ in Infants (V260-035)
NCT01600092 ·Status: COMPLETED ·Phase: PHASE3
-
Effect of Gefapixant on Cough-related Brain Activity in Patients With Chronic Cough
NCT05813223 ·Status: RECRUITING ·Phase: EARLY_PHASE1
-
Safety and Immunogenicity of Norovirus GI.1/GII.4 Bivalent Virus-Like Particle (VLP) Vaccine in Children
NCT02153112 ·Status: COMPLETED ·Phase: PHASE2
-
Safety & Immunogenicity of 1 Dose of GSK134612 in Children 12-14 Months and 3-5 Years Old
NCT00196976 ·Status: COMPLETED ·Phase: PHASE2
-
A Study to Assess the Safety of Live Intranasal Sendai Virus Vaccine in Children and Toddlers
NCT00186927 ·Status: SUSPENDED ·Phase: PHASE1
-
PROtocol for Coxsackievirus VaccinE in Healthy VoluNTteers
NCT04690426 ·Status: COMPLETED ·Phase: PHASE1
-
Determining Reactogenicity and Immunogenicity of Delayed COVID-19 Vaccine Schedule in Children
NCT05329064 ·Status: UNKNOWN ·Phase: PHASE4
-
Efficacy Study With QIVc in Pediatric Subjects
NCT03932682 ·Status: COMPLETED ·Phase: PHASE3
-
Glycophosphopeptical AM3 A Potential Adjuvant in the Treatment of SARS-CoV-2
NCT04987554 ·Status: UNKNOWN ·Phase: NA
-
Effectiveness of Inactivated COVID-19 Vaccine of the First Booster Dose
NCT05367895 ·Status: UNKNOWN
-
Development of a Live Attenuated Rotavirus Vaccine as a Human Infection Challenge Model
NCT04123119 ·Status: COMPLETED ·Phase: NA
-
Evaluating the Comparative Safety and Immunogenicity of Three Lots of Novartis Meningococcal C Conjugate Vaccine in Healthy Toddlers
NCT01434680 ·Status: COMPLETED ·Phase: PHASE2
-
A Study to Evaluate the Safety of Tetravalent Rotavirus Vaccine in Healthy Indian Adult Male Volunteers
NCT01091298 ·Status: COMPLETED ·Phase: PHASE1
-
The Efficacy of Oral Rotavirus Vaccine 116E (ROTAVAC 5D) in Chilean Infants
NCT06200844 ·Status: ACTIVE_NOT_RECRUITING ·Phase: PHASE3
-
Safety, Tolerability and Immunogenicity of Meningococcal B Recombinant Vaccine Administered as Booster Dose at 12, 18 or 24 Months of Age in Toddlers (12-24 Months) Primed With a Three-Dose Immunization Series as Infants in Study V72P12
NCT00944034 ·Status: COMPLETED ·Phase: PHASE2/PHASE3
-
A Study of V260 in Healthy Chinese Adults, Children and Infants (V260-028)(COMPLETED)
NCT00953056 ·Status: COMPLETED ·Phase: PHASE1
-
A Study to Evaluate the Safety, Tolerability, and Immunogenicity of Motavizumab (MEDI-524) After Dosing for a Second Season in Children
NCT00113490 ·Status: COMPLETED ·Phase: PHASE1/PHASE2
-
A Phase 3 Randomized Double Blind Efficacy and Safety Study of Oral Polio Vaccine and NA-831 for Covid-19
NCT04540185 ·Status: UNKNOWN ·Phase: PHASE3