Entamoeba Histolytica Diarrhea
Conditions
Keywords
Entamoeba histolytica, Amebic diarrhea, Nitazoxanide, Metronidazole, Pediatric diarrhea
Brief summary
This randomized controlled trial is comparing two medicines, nitazoxanide and metronidazole, for the treatment of diarrhea caused by Entamoeba histolytica in children. The study is being conducted in the Department of Pediatric Medicine at The Children's Hospital & The Institute of Child Health Sciences, Lahore. A total of 90 children with diarrhea caused by Entamoeba histolytica are included in the study. Participants are randomly assigned to one of two treatment groups. One group receives nitazoxanide, while the other group receives metronidazole. Nitazoxanide is given according to the child's age for 3 days, while metronidazole is given according to body weight for 5 days. The main purpose of the study is to compare how effective the two medicines are in improving diarrhea. Treatment effectiveness is assessed by reduction in stool frequency to three or fewer stools per day and improvement to normal stool consistency. Participants are also assessed for duration of hospital stay and other clinical characteristics. Stool samples are examined after treatment to assess for the presence of Entamoeba cysts or trophozoites. The study aims to determine whether nitazoxanide or metronidazole provides better treatment outcomes in children with Entamoeba histolytica diarrhea.
Detailed description
ntamoeba histolytica is an important cause of intestinal infection and diarrhea in children. Management of amebic diarrhea commonly involves antimicrobial therapy, with metronidazole being a conventional treatment option. Nitazoxanide is another antimicrobial agent that has been used for intestinal parasitic infections. However, comparative evidence regarding their effectiveness in children with Entamoeba histolytica diarrhea remains limited and inconsistent. This randomized controlled trial was conducted to compare the effectiveness of nitazoxanide with metronidazole in children with diarrhea caused by Entamoeba histolytica. The study was conducted in the Department of Pediatric Medicine, The Children's Hospital & The Institute of Child Health Sciences, Lahore. After approval from the Hospital's Ethical Review Board, children fulfilling the study selection criteria were enrolled. A total of 90 participants were included and randomly allocated into two treatment groups using a lottery method, with 45 participants in each group. Written informed consent was obtained from the parents of the participating children. Participants underwent detailed history taking, clinical examination, and relevant laboratory assessment. Children with Entamoeba infection were identified through microscopic examination of stool samples for the presence of cysts or trophozoites. Children with severe dehydration, serious concomitant illness requiring antibiotic treatment, severe adverse events, inability to attend follow-up, or specified systemic disorders were excluded from the study. Participants allocated to the nitazoxanide group received nitazoxanide according to age, while those allocated to the metronidazole group received metronidazole according to body weight. The treatment groups were followed clinically, and information regarding treatment response and clinical outcomes was recorded. Stool samples were collected after completion of therapy and examined microscopically. Clinical assessment was performed by the same consultant pediatrician to maintain consistency in patient assessment and reduce observer-related variation. The principal treatment outcome was effectiveness, assessed by improvement in diarrheal symptoms, specifically reduction of stool frequency to three or fewer stools per day together with normal stool consistency after treatment. Duration of hospital stay was also assessed as an additional clinical outcome. The study further examined whether treatment effectiveness differed according to selected participant characteristics, including age, gender, stool frequency, diarrhea type, and stool consistency. Data were analyzed using SPSS version 26. Numerical variables were summarized using mean and standard deviation, while categorical variables were presented as frequencies and percentages. The Chi-square test was used to compare treatment effectiveness between the two groups, and the independent-samples t-test was used to compare mean duration of hospital stay. Stratified analyses were performed for selected variables to assess potential effect modification. A p-value of ≤0.05 was considered statistically significant. The study included 90 children with a mean age of 6.87 ± 3.28 years. The overall treatment response was higher among participants receiving nitazoxanide than among those receiving metronidazole. In the nitazoxanide group, 41 of 45 participants (91.1%) demonstrated treatment effectiveness, compared with 33 of 45 participants (73.2%) in the metronidazole group, with a statistically significant difference (p=0.040). The mean duration of hospital stay was also shorter in the nitazoxanide group (3.55 ± 1.249 days) than in the metronidazole group (4.57 ± 1.661 days), with a statistically significant difference (p\<0.001). Overall, the findings of the study indicate that nitazoxanide demonstrated a higher treatment effectiveness and shorter hospital stay compared with metronidazole in the studied pediatric population with Entamoeba histolytica diarrhea.
Interventions
Nitazoxanide will be administered orally twice daily for 3 days. Children aged 2-3 years will receive 100 mg per dose, while children aged 4-11 years will receive 200 mg per dose. Treatment will be provided to participants randomized to the nitazoxanide group, with clinical assessment during treatment and follow-up to evaluate treatment efficacy and resolution of diarrhea.
Metronidazole will be administered orally to children diagnosed with Entamoeba histolytica-associated diarrhea. The drug will be given at the recommended pediatric dose according to the child's age and body weight, divided into appropriate daily doses for the prescribed treatment duration. It will serve as the active comparator treatment in the study. Treatment response will be assessed based on clinical improvement, including resolution of diarrhea and other associated symptoms, and compared with the nitazoxanide group.
Sponsors
Study design
Masking description
This is an open-label randomized controlled trial. Participants, treating physicians, study staff, and outcome assessors are not masked to the assigned treatment
Intervention model description
Participants are randomly assigned to one of two parallel treatment groups. Group A receives nitazoxanide, while Group B receives metronidazole. Each participant receives only the assigned treatment.
Eligibility
Inclusion criteria
* Children of both genders aged between 2 to 15 years having diarrhea (frequency of stools greater than 3 or stools softer than normal consistency with nausea, abdominal cramps. Children having Entamoema infection proven on microscopic examination by presence of cyst and trophozite of entamoeba
Exclusion criteria
* Patient with severe dehydration. Patient with any serious concomitant illness that needs antibiotic treatment. If severe adverse events occur at any time. Cytotoxic drugs, food \& chemical poisoning Those who were not able to attend follow-up examinations Children suffering from any other systemic disorders like PEM, certain Immunodeficiencies and Cystic Fibrosis. Microscopic stool examination positive to cyst of Entamoeba histolytica.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Treatment efficacy | Day 5 after initiation of treatment | Treatment efficacy will be assessed by clinical resolution of diarrhea, defined as reduction in diarrheal episodes to three or fewer stools per day together with improvement of stool consistency toward normal after completion of treatment. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Duration of hospital stay | From hospital admission until discharge, assessed up to 5 days after initiation of treatment | Duration of hospital stay will be measured as the total number of days from admission to discharge and compared between the nitazoxanide and metronidazole groups. |
Countries
Pakistan