Viewing Study NCT00367627



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Last Modification Date: 2024-10-26 @ 9:27 AM
Study NCT ID: NCT00367627
Status: COMPLETED
Last Update Posted: 2011-07-12
First Post: 2006-08-22

Brief Title: Relative Efficacy of Two Regimens of Ante-helminthic Treatment
Sponsor: International Centre for Diarrhoeal Disease Research Bangladesh
Organization: International Centre for Diarrhoeal Disease Research Bangladesh

Study Overview

Official Title: None
Status: COMPLETED
Status Verified Date: 2006-08
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The most common soil transmitted helminthic infectionsSTHI includes infection with Ascaris lumbricoides Trichuris trichiura and Hookworm Growth retardation malnutrition anemia impaired cognitive function and immunosuppression are main manifestations in children Even within the developing world wide differences exist in prevalence rates The poorest countries have higher levels of STHI than those with a lower incidence of poverty According to an estimate made by the WHO the prevalence of A lumbricoides T trichiura and Hookworm in South Asia was 27 20 and 16 respectively Given that the prevalence of STHI in urban slums in Bangladesh is much higher than the other parts of the world and Asia and that there are major health and socio-economic consequences of such infections it is important that we come up with effective means of reducing the prevalence of such infections 60-80 of preschool children in urban slums of Bangladesh are infected with these STHI due to poor hygiene At present deworming at six months interval is recommended but the effectiveness of this regimen of dewormig is questionable

2 Hypothesis Ante-helminthic treatment at every three month is more effective than ante-helminthic treatment at every six months to reduce soil transmitted helminthic infection to reduce diarrheal and respiratory illness to improve nutritional status in preschool children

3Objective The main objectives of the proposed study is to compare the relative efficacy of two different ante-helminthic treatment regimens to reduce the prevalence of STHI diarrheal diseases respiratory illness and to improve nutritional status in children 4 Design The population of the study will be preschool children aged 2-5 year and will be selected randomly from an urban of Dhaka They will be divided into two groups randomly One group will get ante-helminthic at every three months interval and the other groups will get at six months interval for one year Stool samples will be collected at the baseline and after three months completing one-year treatment of the above mentioned regimen Blood haemoglobulin and nutritional status will also be measured at baseline and after three months of completion of treatment as mentioned above The treatment will be 400 mg of Albendazole in a single dose

5 Potential Impact The findings of the research can be implemented by the government and non-government organization
Detailed Description: Study design and population

The study population will be the children aged 2-5 years old in the study area All children aged 2-5 years old in one slums of the study area will be listed and will be invited to participate in the study

Parents will be explained the purpose of the study and will be asked for written consent for participation of their children in the study If the parents give the consent then a stool pot will be given to them to collect stool samples for microscopic examination for intestinal parasites The inclusion criteria are 1 age of the child is 2-5 years old 2 heshe has not been suffering from serious chronic illness 3 the child stool test must be positive for STH 4 heshe had not been taken any antehelminthic drug in the previous six months 5 parentsguardian are agree for their child participation in the study The exclusion criteria are 1 age of the child less than 2 years old and more than 5 years old 2 hisher stool test negative for any intestinal helminth 3 heshe has been suffering from serious chronic illness 4 parentsguardian are not willing to give consent for their childs participation in the study 5 if heshe receives any antehelminthic drug after survey but before the study interventions The survey will be done in the first months of the study and then children will be enrolled according to above mentioned inclusionexclusion criteria During screening if any child is found severely malnourished it will be considered asdanger sign according to WHO and IMCI guideline heshe will be referred to an appropriate facility even if shehe is not enrolled in the study Simple randomization technique will be applied to divide the children into two groups A Conventional treatment group who will receive anti-helminthic treatment 400 mg of Albendazole in a single dose at six month interval and B Intervention group who will receive anti-helminthic 400 mg of Albendazole in a single dose treatment at three months interval Stool samples will be collected from both groups prior to anti-helminthic therapy and will be examined quantitatively However stool examination will not be carried out for intestinal parasite after giving 400 mg of Albendazole at 12 months

Sample size calculation

Sample size has been calculated using different predicted values of different out come variables and is shown in the Table 1 A sample size of 200 children 100 in each group will be sufficient for the study

Table 1 Sample size calculation table Indicator Conventional treatment group Intervention treatment group Power of the study 95 CI SD Number in each group Total number adjusted for 10 drop out Cure rate 40 65 90 95 - 78 170 HAZ -2 38 19 90 95 - 84 184 Incidence of E histolytica infection per 100 child-year 20a 15 90 95 10 85 188 Average diarrheal episode per child 2a 1 90 95 15 48 106 Mean haemoglobin mg 10a 12 90 95 4 85 188 Respiratory tract infection episodechild 6a 4 90 95 3 48 106 SD Within group standard deviation

a Data from our ongoing cohort study in Mirpur

Methods

Anthropometric measurement Field Research Assistant will be trained to take weight and height measurement of the children Anthropometric measurements will be taken by trained FRA at the time of enrollment and then every 3-months Each child will be weighed in light clothes with an electronic weighing scale Inter-observer variation up to 25 will be allowed The standing heights of children will be measured to the nearest 01 cm using a locally constructed height stick Again inter-observer variation up to 25 will be allowed Nutritional status will be assessed by comparing the weight and height of the study children with those of NCHS reference population of the same age and sex with the help of Epi6 computer package program and weight for age Z score WAZ and height for age Z score HAZ will be computed 29 Malnourished and stunted will be defined by the WAZ score and HAZ score -2 respectively

Other disease morbidity Each study subject will be visited by a community health worker every week and will collect information by asking parentsguardian according to structured questionnaires about diarrheal disease fever cough etc of the child retrospectively for previous seven days They will work 6 days weekly and every one of them has to visit about 17 households per day for morbidity data collection Parentsguardian will be advised to seek health care from study physician in study field office in case of any illness of the study child The study physician will take history and will carry out physical examination and will give treatment to the sick child If the child does not respond to the given treatment or if hisher condition deteriorates or if the child is seriously ill initially then heshe will be referred to the appropriate referral facilities for treatment and treatment cost will not be carried out by the project Asymptomatic E histolytica infections will not be treated But symptomatic E histolytica infections will be treated according to the ICDDR B Dhaka Hospital treatment guidelines

Intestinal helminth infections induce Th-2 immune response 27 which might favor others viral bacterial and protozoan infections De-worming has been shown to improve antibody response 28 In our ongoing cohort study in Mirpur it has been found that children with heavy Trichuris trichiura TT infections suffered significantly more from E histolytica associated infection un published data compare to those children with light infection with TT Based on these observations it can be hypothesized that a frequent de-worming regimen will be associated with less other disease morbidtity like diarrheal diseases respiratory infections and intestinal protozoan infections with E histolytica Clinical definitions Diarrhea was defined as having three or more unformed stools in a 24 hour period A diarrheal episode was defined as being separated from another episode by at least 3 diarrhea-free days

Respiratory tract infection defined as a Perceptions of a child who has a cough is breathing faster than usual with short quick breaths or is having difficulty breathing excluding children that had only a blocked nose 30 No attempt will be done to identify the etiology of the respiratory infection

Cure rate of STH infection CR Cure rate from STH infection is defined as follows

Prevalence before at enrollment - prevalence at the end of the study CR --------------------------------------------------------------------------------------------- x 100
Prevalence before at enrollment

Laboratory methods

Blood hemoglobin measurement Study physician will measure blood hemoglobin of the child at enrollment and at the end of the study period by hemocytometer at field site 31

Stool parasite examination The community health workers will collect stool samples for qualitative and quantitative intestinal parasite measurement at every three months interval The stool will be examined by conventional microscopy for qualitative measurement and for quantitative measurement of intestinal helminthes by Kato-Katz or Formalin-ether concentration technique will be used 32E histolytica will be detected by stool microscopy and ELISA as described by R Haque el at33

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None