High Amylose Maize Starch for Treatment of Cholera

Diarrhea Clinical Trial

— RESTORS  

Official title:

Phase 2, Single Centre, Randomized, Double-blind Study Conducted in Adult Males With Acute Dehydrating Diarrhea Due to Cholera With the Aim Being to Select One or More of the Three Fermentable Starches (FS) for an FS-HO-ORS Formulation.

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT01823952
• Other study ID #: RESTORS
• Status: Terminated
• Phase: N/A
• First received: March 27, 2013
• Last updated: April 2, 2014
• Start date: April 2013
• Est. completion date: February 2014

Study information

• Verified date: February 2014
• Source: PATH
• Contact: n/a
• Is FDA regulated: No
• Health authority: Bangladesh: Bangladesh Medical Research CouncilBangladesh: Directorate of Drug AdministrationBangladesh: Ethical Review CommitteeUnited States: Institutional Review Board
• Study type: Observational

Clinical Trial Summary

A randomized, double-blind trial in adult males with acute dehydrating diarrhea of cholera comparing the safety, tolerability and efficacy of HAMS HO-ORS, HAMS 2.5% Acetate HO-ORS, HAMS 6% Acetate HO-ORS and HO-ORS.

The primary hypothesis is that at least one of the hypo-osmolar ORS containing high amylose maize starch 6% acetate (HAMSA6-HO-ORS), hypo-osmolar ORS containing high amylose maize starch 2.5% acetate (HAMSA2.5-HO-ORS) and a hypo-osmolar ORS containing high amylose maize starch (HAMS-HO-ORS), will significantly reduce diarrhea duration compared with hypo-osmolar (HO) ORS.

Specifically, the investigators expect that HAMSA6 will be the most effective preparation.

Description:

• Burden: Watery diarrhea including cholera continues to be a major cause of childhood mortality in developing countries, with an estimated 1.5 million children dying each year. This figure has greatly reduced from approximately 5 million diarrheal deaths annually 20 years ago, a phenomenon often attributed to the utilization of oral rehydration solution (ORS).

• Knowledge Gap: ORS is very effective in correcting dehydration and reducing mortality, but is not adequately used in many countries, partly due to the fact that it does not reduce diarrhea. The physiological basis for ORS is that glucose-stimulated sodium and fluid absorption is not inhibited by cyclic 3',5'-adenosine monophosphate (cAMP) and other diarrhea mediators which inhibit sodium chloride absorption. The conventional glucose-based ORS does not reduce duration or severity of diarrhea and may in fact paradoxically increase fecal fluid losses. Advances in ORS composition have included the universal adoption of hypo-osmolar ORS (HO-ORS) in 2003. Recent technological innovations have led to the use of amylase-resistant starches and their modifications in the treatment of diarrhea. Short chain fatty acids (SCFA), which are produced in colon from these non-absorbed carbohydrates, enhance sodium absorption. An orally administered, non-absorbed starch (i.e., one resistant to digestion by amylase) significantly reduced fecal fluid loss and the duration of diarrhea in patients with cholera.

• Relevance: Efforts are continuing to improve the efficacy of oral rehydration solution. As glucose stimulates sodium and water absorption in small intestine, short chain fatty acids (SCFAs) stimulate sodium and water absorption in the colon. In cholera, colonic function is also impaired due to the lack of SCFAs. The main source of SCFAs is the unabsorbed carbohydrates that are fermented in the colon by the colonic bacteria. The maize starch contains substantial amount of amylase resistant starch that escapes digestion and absorption in the small intestine and is fermented in the colon, liberating SCFAs. We expect that our experimental ORS containing maize starch will reduce the severity (stool volume) and enhance recovery (reduce duration) of diarrhoea.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 106
• Est. completion date: February 2014
• Est. primary completion date: February 2014
• Accepts healthy volunteers: No
• Gender: Male
• Age group: 18 Years to 65 Years

Eligibility

INCLUSION CRITERIA:

A participant is considered eligible for participation in the trial if the following inclusion criteria are satisfied on admission (Day 1, before randomization) to the hospital:

1. Participant is a male between 18 and 65 years of age inclusive

2. Severe watery diarrhea without fecal blood of less than 48 hours (with passage of 3 or more watery stools in the 24 hours before admission)

3. Signs of severe dehydration as per ICDDR,B guidelines (modified WHO guideline)

4. Dipstick test/Dark-field examination positive for Vibrio cholera

5. Written informed consent is provided

6. Participant is willing and able to comply with all trial requirements

EXCLUSION CRITERIA:

A participant who meets any of the following criteria on admission (before randomization) to the hospital will not qualify for the study

1. Evidence or history of any clinically significant illness as per the Investigator's discretion.

2. Known case of HIV or Hepatitis B

3. History of cancer

4. Known renal disease

5. Frequent excessive alcohol use, binge drinking (e.g. men consume 5 or more drinks in about 2 hours) or use of illicit drugs within the past two years

6. History of receiving antimicrobial or anti-diarrheal medication (loperamide, diphenoxylate, etc.) within seven days of admission

7. Concomitant infection requiring antimicrobial therapy

8. Donated blood or plasma or experienced clinically significant loss of blood within eight weeks prior to admission or who plan to donate blood within 1 month after study participation

9. Clinically significant abnormal laboratory test results as determined by the investigator

10. Treatment within 30 days prior to admission (or five half-lives of the compound, if longer) with any investigational agent or device

11. History of seizure (including febrile seizure) or loss of consciousness;

12. History of any GI Surgery related to Bowel resections and gastric anastomoses in past except Appendicitis

13. For any reason, deemed by the investigator to be inappropriate for this study, including participants who are unable to communicate or to cooperate with the investigator or designee

14. Prior enrolment in this trial

Study Design

N/A

Related Conditions & MeSH terms

• Cholera
• Diarrhea

Locations

Country	Name	City	State
Bangladesh	Dhaka Hospital - icddr,b (International Centre for Diarrhoeal Disease Research, Bangladesh)	Mohakhali	Dhaka

Sponsors (1)

Lead Sponsor	Collaborator
PATH

Country where clinical trial is conducted

Bangladesh, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Safety & Tolerability as measured by adverse events, vital signs and lab parameters	Proportion of patients with biochemical and symptomatic hyponatremia; Proportion of patients with adverse events deemed possibly or definitely related to treatment with the investigational products; Proportion of patients with abnormal biochemical and haematological values (any grade 3 as per CTCAE version IV criteria or above); Proportion of patients with serious adverse events deemed possibly or definitely related to treatment with investigational products	Approximately 24 hours after randomization	Yes
Primary	Duration of Diarrhea	Criteria evaluated: Duration of diarrhea during the study period (defined as time from randomisation to the last watery stool preceding two soft/formed stools or a 12 hour period without diarrhea, up to a maximum of 96 hours)	12 hrs w/o diarrhoea, up to max of 96 hrs	No
Secondary	Stool output and fluid intake rate	Criteria evaluated: Total output of watery stool (g/kg body weight); Weight of watery stool; Intake of oral fluids including ORS and plain water in mL/kg from time of randomization to the first soft/formed stool or 48 hours of treatment with study products, whichever is sooner; Proportion of patients who vomit in the first 24 hours; Proportion of patients who require unscheduled intravenous fluids post randomization; Amount (mL/kg) of unscheduled intravenous fluids required post randomization; Proportion of patients with diarrhea beyond 48 hours	0 to 96 hrs	No