Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02486835
Other study ID # ABO-cough-2015
Secondary ID
Status Completed
Phase N/A
First received May 17, 2015
Last updated January 25, 2018
Start date December 23, 2015
Est. completion date April 6, 2016

Study information

Verified date January 2018
Source Clalit Health Services
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Cough is a life saving reflex, therefore it is important, especially in pediatrics, to calm cough spells without sedating the reflex. The intent of this study is to use a protective syrup with does not act as a sedative or as a potent mucolytic and measure its efficacy and safety versus placebo in children with moderate to severe night and daily cough. Cough is assessed with a validated parent questionnaire. The degree of disturbance of cough is followed immediately after one night administration of the study products and daily for 4 nights, 3 days.


Description:

Cough is a life saving reflex, therefore it is important, especially in pediatrics, to calm cough spells without sedating the reflex. Looking into mechanisms for cough management different from mucolytics, or sedatives, such as protection of irritated pharynx mucosa from post nasal drip or other irritating substances is theoretically sound and shows practical interesting results.

A parallel comparison of efficacy and tolerability between such protective mechanism (acting through a barrier and radical scavenging action) due to natural substances (honey, plantago lanceolata and thymus vulgaris) and placebo has not been done so far, in very young children, especially in a time frame of 4 days. The intent of this study is to use the protective syrup versus placebo in children with moderate to severe night and daily cough, measured with a validated parent questionnaire. The degree of disturbance of cough is followed immediately after one night administration of the study products and daily for 4 nights, 3 days.

Assessment of effectiveness of the protective cough syrup as compared to placebo is considered very interesting due to the mechanism of the remedy.


Recruitment information / eligibility

Status Completed
Enrollment 150
Est. completion date April 6, 2016
Est. primary completion date April 3, 2016
Accepts healthy volunteers No
Gender All
Age group 1 Year to 5 Years
Eligibility Inclusion Criteria:

- cough attributed to infection of the upper respiratory tract since less or equal than 7 days,

- children aged 1 to 5 years

- score of three or more of al least two of the following three questions relating to night cough, frequency of nocturnal cough, impact on sleep of child and impact on sleep of parent,

- score of at least three of all questions assessing daytime cough considering the day prior to study entry

- written consent by a parent.

Exclusion Criteria:

- Children with a diagnosis of acute laryngotracheal bronchitis, pneumonia, asthma, sinusitis, allergic rhinitis, as well as chronic cardiac condition, or cystic fibrosis or any anatomical respiratory tract anomalies,

- Children who received antihistamines or any cough medicine the day prior to study entry,

- The administration of any steroid preparation by oral administration or inhalation on the day prior to study entry,

- Known sensitivity to any component of placebo or to Plantago lanceolata or Thymus vulgaris, honey or any other component of the cough syrup.

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Cough syrup for adults and children
Dosage is 5 ml three times a day for 4 nights, 3 days
Placebo
Dosage is 5 ml three times a day for 4 nights, 3 days

Locations

Country Name City State
Israel Pediatric Ambulatory Clinic Bat-Yam Bat Yam
Israel Pediatric Ambulatory Clinic Kfar-Saba Kfar Saba
Israel Pediatric Community Ambulatory Clinic - Petach-Tikva Peta? Tiqwa
Israel Pediatric Ambulatory Clinic Ramat Aviv Gimel Tel Aviv

Sponsors (1)

Lead Sponsor Collaborator
Clalit Health Services

Country where clinical trial is conducted

Israel, 

References & Publications (9)

Bogdanov S, Jurendic T, Sieber R, Gallmann P. Honey for nutrition and health: a review. J Am Coll Nutr. 2008 Dec;27(6):677-89. Review. — View Citation

Canciani M, Murgia V, Caimmi D, Anapurapu S, Licari A, Marseglia GL. Efficacy of Grintuss® pediatric syrup in treating cough in children: a randomized, multicenter, double blind, placebo-controlled clinical trial. Ital J Pediatr. 2014 Jun 10;40:56. doi: 10.1186/1824-7288-40-56. — View Citation

Cohen HA, Rozen J, Kristal H, Laks Y, Berkovitch M, Uziel Y, Kozer E, Pomeranz A, Efrat H. Effect of honey on nocturnal cough and sleep quality: a double-blind, randomized, placebo-controlled study. Pediatrics. 2012 Sep;130(3):465-71. doi: 10.1542/peds.2011-3075. Epub 2012 Aug 6. — View Citation

Middleton KR, Hing E. National Hospital Ambulatory Medical Care Survey: 2004 outpatient department summary. Adv Data. 2006 Jun 23;(373):1-27. — View Citation

Paul IM, Beiler J, McMonagle A, Shaffer ML, Duda L, Berlin CM Jr. Effect of honey, dextromethorphan, and no treatment on nocturnal cough and sleep quality for coughing children and their parents. Arch Pediatr Adolesc Med. 2007 Dec;161(12):1140-6. — View Citation

Paul IM, Yoder KE, Crowell KR, Shaffer ML, McMillan HS, Carlson LC, Dilworth DA, Berlin CM Jr. Effect of dextromethorphan, diphenhydramine, and placebo on nocturnal cough and sleep quality for coughing children and their parents. Pediatrics. 2004 Jul;114(1):e85-90. — View Citation

Rimsza ME, Newberry S. Unexpected infant deaths associated with use of cough and cold medications. Pediatrics. 2008 Aug;122(2):e318-22. doi: 10.1542/peds.2007-3813. — View Citation

Schramm DD, Karim M, Schrader HR, Holt RR, Cardetti M, Keen CL. Honey with high levels of antioxidants can provide protection to healthy human subjects. J Agric Food Chem. 2003 Mar 12;51(6):1732-5. — View Citation

Wegener T, Kraft K. [Plantain (Plantago lanceolata L.): anti-inflammatory action in upper respiratory tract infections]. Wien Med Wochenschr. 1999;149(8-10):211-6. Review. German. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Change in night cough frequency score in the general population Night cough frequency is the most invasive element of distress to the child and family. The questionnaire rating night cough is filled in each morning relating to the passed night for four nights. The basal night score is the score of the night before enrollment. baseline up to night 1
Secondary Change in night cough frequency score in the population coughing since 1-2 days All these other elements constitute cough invasiveness into the quality of life of child and parents baseline up to night 1
Secondary Change in night cough frequency score in the female population coughing since 1-2 days All these other elements constitute cough invasiveness into the quality of life of child and parents baseline up to night 1
Secondary Change in night cough frequency score in the male population coughing since 1-2 days All these other elements constitute cough invasiveness into the quality of life of child and parents baseline up to night 1
Secondary Change in night cough severity score in the general population All these other elements constitute cough invasiveness into the quality of life of child and parents baseline up to night 1
Secondary Change in night cough severity score in the population coughing since 1-2 days All these other elements constitute cough invasiveness into the quality of life of child and parents baseline up to night 1
Secondary Change in night cough bothersomeness score in the general population All these other elements constitute cough invasiveness into the quality of life of child and parents baseline up to night 1
Secondary Change in night cough bothersomeness score in the population coughing since 1-2 days All these other elements constitute cough invasiveness into the quality of life of child and parents baseline up to night 1
Secondary Change in night cough influence on sleep of child score in the general population All these other elements constitute cough invasiveness into the quality of life of child and parents baseline up to night 1
Secondary Change in night cough influence on sleep of child score in the population coughing since 1-2 days All these other elements constitute cough invasiveness into the quality of life of child and parents baseline up to night 1
Secondary Change in night cough influence on sleep of parent score in the general population All these other elements constitute cough invasiveness into the quality of life of child and parents baseline up to night 1
Secondary Change in night cough influence on sleep of parent score in the population coughing since 1-2 days All these other elements constitute cough invasiveness into the quality of life of child and parents baseline up to night 1
Secondary Change in night cough combined score in the general population All these other elements constitute cough invasiveness into the quality of life of child and parents baseline up to night 1
Secondary Change in night cough combined score in the population coughing since 1-2 days All these other elements constitute cough invasiveness into the quality of life of child and parents baseline up to night 1
Secondary Change in day cough frequency score in the general population The questionnaire rating day cough is filled in each evening relating to the passed day for three days.
The basal day score is the score of the day before enrollment.
baseline up to day 2
See also
  Status Clinical Trial Phase
Completed NCT00116337 - Spinal Cord Stimulation to Restore Cough N/A
Not yet recruiting NCT04064333 - Slow-Stream Expiratory Muscle Strength Training for Veterans With Dysphagia Living in Long-term Care N/A
Recruiting NCT02482818 - Efficacy of Pregabalin on Chronic Cough Phase 1/Phase 2
Terminated NCT02269761 - Chest Ultrasound of ER Patients With Cough or SOB
Active, not recruiting NCT02065440 - The Effect of Ebastine/Pseudoephedrine on Subacute Cough N/A
Completed NCT01071161 - The Effect of Azithromycin in Patients With Chronic Obstructive Pulmonary Disease (COPD) and Chronic Productive Cough Phase 3
Terminated NCT00668317 - Bronchial Hyper-responsiveness in Reflux Cough Phase 3
Completed NCT00353951 - An Observational Study of Cough / Lower Respiratory Tract Infection (LRTI) in Primary Care N/A
Completed NCT00127686 - Effect of Honey and Dextromethorphan on Nocturnal Cough and Sleep Phase 1
Completed NCT00287339 - The Utility of Nexium in Chronic Cough and Reflux Disease Phase 4
Recruiting NCT05115097 - AI Evaluation of COVID-19 Sounds (AI-EChOS)
Recruiting NCT04457011 - Efficacy and Safety of Susu Zhike Granules for Treating Acute Cough Due to Common Cold With Cold-cough Syndrome in Children Phase 2
Recruiting NCT05042063 - Acoustic Cough Monitoring for the Management of Patients With Known Respiratory Disease
Recruiting NCT03922373 - A Study of Benzonatate Soft Capsule in Chinese Healthy Subjects Phase 1
Completed NCT05812209 - Stellate Ganglion Block to Treat Long COVID 19 Case Series
Recruiting NCT04767074 - A Non-pharmacological Cough Control Therapy N/A
Recruiting NCT05570539 - Assessment of the Pharmacokinetics of BLU-5937 Extended Release Prototypes and a BLU-5937 Immediate Release Reference Formulation Phase 1
Completed NCT03999203 - A Cross-sectional Study to Measure Cough in Severe Asthma N/A
Active, not recruiting NCT05479929 - Work of Breathing Assessment in Triage Scale
Recruiting NCT02495571 - Assessment of Voluntary and Reflex Cough in Patients With ALS N/A