Cette page a été traduite automatiquement et l'exactitude de la traduction n'est pas garantie. Veuillez vous référer au version anglaise pour un texte source.

Senna vs. Polyethylene Glycol 3350 for the Treatment of Retentive Encopresis in Children

17 juin 2026 mis à jour par: Yogev Dotan, Shaare Zedek Medical Center

Senna vs. Polyethylene Glycol 3350 for the Treatment of Retentive Encopresis in Children: a Randomized, Double-blinded, Study

The goal of this clinical trial is to learn which treatment is more effective for children with functional constipation (FC) and fecal incontinence (FI), also called retentive encopresis.

Functional constipation is common in children and can cause pain, embarrassment, social stress, and repeated medical visits. One of the hardest symptoms to treat is fecal incontinence. Two common treatments are polyethylene glycol 3350 (PEG), an osmotic laxative, and Senna, a plant-based stimulant laxative. PEG is often used as standard maintenance therapy, while Senna is increasingly used, especially in children with difficult or refractory constipation. However, there is not enough high-quality evidence comparing these two treatments directly in children with fecal incontinence.

The main question this study aims to answer is:

Does Senna reduce the number of fecal incontinence episodes more than PEG after 3 months of treatment? The study will also assess safety, tolerability, abdominal pain or cramping, use of rescue enemas, treatment satisfaction, and treatment compliance.

This is a prospective, randomized, double-blinded clinical trial. Children will be randomly assigned to receive either daily Senna or daily PEG for 3 months. Neither the families nor the treating medical team will know which treatment the child is receiving. Both medications will be prepared as identical-looking white powder in identical packages.

Participants will be children aged 4 to 18 years who have functional constipation according to Rome IV criteria and have fecal incontinence at least 4 times per week. Children with an organic disease that may cause fecal incontinence, such as Hirschsprung disease, spinal cord abnormalities, or anorectal malformations, will not be included.

Before starting the study medication, all participants will complete a 3-day bowel clean-out using high-dose PEG, with Pico-Salax added on the third day. After this clean-out, children will start their assigned daily treatment, either Senna or PEG. The dose will be based on age and may be adjusted by the physician according to stool consistency, stool frequency, cramping, and the child's clinical response. All families will also receive behavioral advice, including regular toilet sitting twice daily, correct toilet position using a footstool, and going to the toilet when the child feels the need.

Participants will:

  • Take daily Senna or daily PEG for 3 months
  • Visit the clinic at baseline, 1 month, 2 months, and 3 months
  • Complete a 7-day stool and fecal incontinence diary before each visit
  • Report abdominal pain, cramping, diarrhea, perianal irritation, or any other adverse events
  • Return medication containers so compliance can be checked by weighing the remaining medication
  • Complete satisfaction and improvement questionnaires at the 3-month visit

Outcome Measurements:

The primary outcome is the mean number of fecal incontinence episodes per week after 3 months of treatment. This will be measured using a prospective 7-day diary completed by the family before the 3-month clinic visit.

The secondary outcomes, assessed at 3 months, include:

  • Change in patient-initiated toilet sitting, meaning times when the child independently says they need to defecate
  • The proportion of children who reach 0-1 fecal incontinence episodes per week
  • The proportion of children with any improvement, defined as at least 1 fewer fecal incontinence episode per week
  • Number of rescue enemas used during the 3-month study period
  • Frequency and severity of abdominal pain or cramping
  • Parent-reported satisfaction with treatment using a 5-point Likert scale
  • Family impression of overall improvement using a 5-point Likert scale
  • The proportion of children still meeting Rome IV criteria for functional constipation
  • Treatment compliance, defined as good compliance if more than 80% of doses were taken

The study plans to enroll 80 children total, with 40 children in the Senna group and 40 children in the PEG group.

Aperçu de l'étude

Type d'étude

Interventionnel

Inscription (Estimé)

80

Phase

  • Première phase 1

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Coordonnées de l'étude

Sauvegarde des contacts de l'étude

Lieux d'étude

      • Be’er Ya‘aqov, Israël
        • Shamir Medical Center
        • Contact:
          • Adi Ein Dor
      • Jerusalem, Israël, 91031
        • Shaare Zedek Medical Center
        • Contact:
        • Chercheur principal:
          • Dotan Yogev, MD

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

  • Enfant

Accepte les volontaires sains

Non

La description

Inclusion Criteria:

  • Children aged 4 to 18 years.
  • Diagnosis of functional constipation according to Rome IV criteria.
  • Fecal incontinence occurring ≥4 times per week.
  • Treatment-naïve or treatment-experienced (i.e., any of the following treatments in the past: PEG, senna, bisacodyl and rectal disimpaction) patients.

Exclusion Criteria:

  • Presence of organic disease that causes or contributes to fecal incontinence (e.g., Hirschsprung disease, spinal cord anomalies, anorectal malformations).

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Traitement
  • Répartition: Randomisé
  • Modèle interventionnel: Affectation parallèle
  • Masquage: Tripler

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Comparateur actif: PEG 3350

Patients assigned to the PEG group will receive age-based dosing according to standard clinical guidelines, with flexibility for dosing adjustments. Each container will contain an identical white powder and a measuring spoon. One measuring spoon will contain 17g of PEG. Initial dosing will be according to age groups as follows:

  • 4-7 years: ½ spoon, once daily
  • 8-18 years: 1 spoon, once daily
Comparateur actif: Senna

Patients assigned to the Senna group will receive age-based dosing, in line with standard clinical guidelines and clinical practice. Dosing adjustments will be permitted and encouraged throughout the trial based on physician judgment at clinical visits or family-initiated requests. Each container will contain an identical white powder and a measuring spoon. One measuring spoon will contain 20mg of Senna. Initial dosing will be according to age groups as follows:

  • 4-7 years: ½ spoon, once daily
  • 8-18 years: 1 spoon, once daily

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Number of fecal incontinence incidents per week at 3 months
Délai: At 3 months
Mean number of fecal incontinence episodes per week at 3 months of treatment. A prospective 7-day diary will be completed by the family, at enrollment and before each monthly visit. The 3-month clinic meeting diary will be used to measure this outcome.
At 3 months

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Proportion of patients achieving 0-1 fecal incontinence episodes per week.
Délai: At 3 months
At 3 months
Proportion of patients achieving any improvement (≥1 episode/week reduction)
Délai: At 3 months
At 3 months
Number of enemas used during the 3-month period
Délai: From enrollment till 3 months
From enrollment till 3 months
Proportion of patients experiencing mild versus moderate-to-severe abdominal pain or cramping (classified by physician and family report).
Délai: From enrollment till 3 months
From enrollment till 3 months
Proportion of patients still meeting Rome IV criteria for functional constipation
Délai: At 3 months
At 3 months
Compliance Assessment: Compliance with assigned treatment will be assessed based weighing the medication containers: Classification as "good compliance" (>80% doses taken) versus "poor compliance" (<80%)
Délai: From enrollment till 3 months
From enrollment till 3 months
Change in patient-initiated toilet-sitting
Délai: At 3 months
Improvement in patient-initiated toilet-sitting: To understand changes in bowel habits, the study will distinguish between parent-initiated toilet sitting ("it's time to go to the bathroom/I think you need to poop") and patient-initiated toilet sitting ("I need to go!"). Changes in the number of patient-initiated sittings/week throughout the study will be compared between both treatments.
At 3 months
Parent-reported satisfaction with treatment
Délai: At 3 months
Parent-reported satisfaction with treatment will be measured on a 5-point Likert scale from "Very Satisfied" to "Very Dissatisfied".
At 3 months
Family impression of overall improvement
Délai: At 3 months
Family impression of overall improvement will be measured on a 5-point Likert scale from "Very Satisfied" to "Very Dissatisfied".
At 3 months

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Estimé)

1 juillet 2026

Achèvement primaire (Estimé)

1 juillet 2027

Achèvement de l'étude (Estimé)

1 janvier 2028

Dates d'inscription aux études

Première soumission

17 mai 2026

Première soumission répondant aux critères de contrôle qualité

17 mai 2026

Première publication (Réel)

22 mai 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

18 juin 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

17 juin 2026

Dernière vérification

1 juin 2026

Plus d'information

Termes liés à cette étude

Plan pour les données individuelles des participants (IPD)

Prévoyez-vous de partager les données individuelles des participants (DPI) ?

INDÉCIS

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Non

Étudie un produit d'appareil réglementé par la FDA américaine

Non

produit fabriqué et exporté des États-Unis.

Non

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

S'abonner