Safety, Tolerability and Preliminary Efficacy of Lenodiar Pediatric in Diarrhea

Diarrhea Clinical Trial

Official title:

Safety, Tolerability and Preliminary Efficacy of Oral Administration of Tannins and Flavonoids in the Management of Pediatric Diarrhea

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT03598010
• Other study ID #: ABO-LEN-02/19
• Status: Not yet recruiting
• Phase: N/A
• Start date: October 2019
• Est. completion date: March 2021

Study information

• Verified date: May 2019
• Source: Aboca Spa Societa' Agricola
• Contact: Niccolò Ravenni, PhD
• Phone: +39 0575 746
• Email: clinicaltrials[@]aboca.it
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Evaluation of the efficacy of a treatment with Actitan-F, a natural molecular complex of tannins (from Agrimony and Tormentil) and flavonoids (Chamomile) in a pediatric population of children affected by acture/prolonged/chronic diarrhea

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 240
• Est. completion date: March 2021
• Est. primary completion date: December 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: 1 Year to 12 Years

Eligibility

Inclusion Criteria

1. Children of either sex aged between 1-12 years (inclusive);

2. Evidence of acute (onset <7 days prior to screening visit), prolonged (onset between 7 and 14 days prior to screening visit) or chronic (onset >14 days prior to screening visit) diarrhea.

• Acute/Prolonged Diarrhea is defined as at least 3 evacuations of loose or watery stools (stools type 6-7 of Bristol scale) occurring in the 24 hours preceding the screening visit.

• Chronic Diarrhea (>14 days duration), defined by passage of loose or watery stools (Bristol score 6 or 7) with or without an increase in frequency of bowel movements;

3. Evidence of mild to moderate dehydration, defined as a score 1-4 in the Clinical Dehydration Scale;

4. Parents/legal guardians availability to fill on a daily basis the electronic daily diary by a smartphone/tablet/laptop.

5. Parents/legal guardians* have given a written informed consent for participation in the study at the time of enrolment or before. The parent/legal guardian should also have agreed to bring the child for the visits scheduled in the protocol and to provide the requested information during the telephonic follow-up visit;

6. Parents/legal guardian able to understand the full nature and the purpose of the investigation, including possible risks and side effects, able to cooperate with the Investigator and to comply with the requirements of the entire investigation (ability to attend all the planned investigation visits according to the time limits included) based on Investigator's judgement.

Exclusion Criteria:

Exclusion Criteria

1. Children of female sex having started menarche;

2. Evidence of severe dehydration, defined as a score > 4 in the Clinical Dehydration Scale;

3. Known hypersensitivity to any of the components (active ingredients or excipients) of the investigational product;

4. Severely malnourished patients, defined as those patients with body weight < 50% for age;

5. History of immune diseases or conditions known to producing immunodeficiency (AIDS, other congenital immunodeficiency syndromes, anticancer drugs, etc.);

6. For acute/prolonged diarrhea only, patients who have received any of the following treatments within the 2 weeks before the screening/baseline visit:

• Drugs with adsorbing properties, e.g. kaolin, pectin, bismuth subsalicylate;

• Drugs that modify intestinal secretions, e.g. racecadotril;

• Drugs that modify intestinal motility, e.g. opiates such as loperamide, atropine and other anti-cholinergic agents);

• Laxatives

• Antibiotics

7. History of seizures due to known or unknown causes;

8. Parents/legal guardians' refusal or inability to give written informed consent to participate in the study;

9. Parents/legal guardians who, in the opinion of the Investigator, are unable to fill up the electronic patient diary;

10. Patients who may not be possible to come for the scheduled visits;

11. Patients who have participated in any other clinical trial in the last 3 months prior to the start of the study.

Related Conditions & MeSH terms

• Acute Diarrhea
• Chronic Diarrhea
• Diarrhea
• Diarrhea, Infantile

Intervention

Device:
• Actitan-F (7dd)
1 sack every 4 hours, maximum 4 sacks/day for 7 days.
• Actitan-F (28dd)
1 sack every 4 hours, maximum 4 sacks/day for 28 days.

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Aboca Spa Societa' Agricola

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Acute (onset <7 days) or Prolonged Diarrhea (onset =7 and =14 days): Response Rate (RR) measured after 4 treatment days.	Acute (onset <7 days) or Prolonged Diarrhea (onset =7 and <14 days): Response Rate (RR) measured after 4 treatment days. Patients will be considered as responders if they have experienced the passage of 2 formed stools or no stool for at least 12 consecutive hours during the 4 days treatment.	Day0 to Day4
Primary	Chronic Diarrhea (onset >14 days): Response Rate (RR) measured across the whole treatment period	Chronic Diarrhea (onset >14 days): Response Rate (RR) measured across the whole treatment period (4 weeks). Patients will be considered as responders if they have experienced a 50% (or more) reduction in the number of days with at least 1 diarrheic stools (Bristol score 6 or 7) in the whole treatment period (4 weeks) compared to the 7 days prior the treatment (baseline).	Day0 to Day28
Secondary	Number of episodes of daily watery evacuations	Number of episodes of daily watery evacuations evaluated by means of the electronic patient diaries;	Day0-Day28
Secondary	Number of unformed stools passed per 24-h interval, after the first dose	Number of unformed stools passed per 24-h interval, after dosing evaluated by means of the electronic patient diaries	Day0-Day28
Secondary	Number of treatment failures	Number of treatment failures. A treatment failure is defined as clinical deterioration or worsening of symptoms or illness continuing after 120 h following the first dose evaluated by means of the electronic patient diaries	Day0-Day28
Secondary	Difference in body weight	Difference in body weight between baseline and End of Treatment	Day0-Day28
Secondary	Frequency and severity of diarrhea associated symptoms	Frequency and severity of diarrhea associated symptoms (nausea, vomiting, abdominal pain). Severity will be evaluated by means of a 0-4 Likert scale (0 = none; 1 = mild; 2 = moderate; 3 = severe; 4 = very severe);	Day0-Day28
Secondary	Treatment Compliance	Evaluation of the nr of sachets prescribed by the investigators and the % of compliance recorded	Day0-Day28
Secondary	Proportion of patients requiring other (allowed) treatments	Proportion of patients requiring other treatments in addition to Lenodiar Pediatric or to other concomitant treatments prescribed at baseline visit for diarrhea symptoms relief (e.g. parenteral rehydration and/or other medications) evaluated by means of the electronic patient diaries	Day0-Day28
Secondary	Change in results of the Pediatric Quality of Life Questionnaire (PedsQL)	Change in results of the Pediatric Quality of Life Questionnaire (PedsQL) between baseline and End of Treatment visits	Day0-Day28
Secondary	Change in results in parent assessment of children Quality of Life (100 mm VAS)	Change in results in parent assessment of children Quality of Life (100 mm VAS) between baseline and End of Treatment visits	Day0-Day28
Secondary	Safety and tolerability of the treatment: Incidence of adverse events (AEs) and serious adverse events (SAEs), and rate of study discontinuations due to AEs/SAE;	Incidence of adverse events (AEs) and serious adverse events (SAEs), and rate of study discontinuations due to AEs/SAE;	Day0-Day28