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ReclutandoNCT07927907Registro de ClinicalTrials.gov

A Clinical Trial to Evaluate the Effects of a Supplement on Gut Health

Gut Health · Bloating · Digestive Discomfort · Constipation · Diarrhea · Heartburn · Abdominal Pain · Gasiness

LO ESENCIAL

De qué trata este estudio

El registro indica que este estudio recluta participantes. La disponibilidad puede variar por centro.

Tipo de estudio
De intervención
Fase
No aplica
Rango de edad
18 años - 60 años
Sexo admitido
Todos los sexos
Voluntarios sanos
No aceptados
Participantes
40 Estimado

Estos son puntos de partida, no una decisión de elegibilidad. El equipo debe revisar todos los requisitos.

Las explicaciones y la navegación están en español. Los textos proporcionados por el registro, incluidos títulos, resúmenes y criterios, se conservan en su idioma original. Puedes pedir orientación en español a WCR.

Acerca de la investigación

This study will evaluate the effects of the Peachbiotic supplement on gut health in adults experiencing gastrointestinal symptoms. The trial is a single-arm, open-label, virtual study in which all 40 enrolled participants will use the test product daily for 12 weeks.

Participants will take one capsule of the product once daily in the morning with food and will complete self-reported questionnaires at Baseline, Week 4, Week 8, and Week 12 to assess changes in gut health outcomes including bloating, digestive comfort, regularity of bowel movements, gasiness, and general well-being.

¿Quién podría participar?

La lista siguiente contiene el texto del patrocinador. Puede incluir condiciones, tratamientos previos, resultados de pruebas y otros requisitos. Aparecer en tu búsqueda no significa que califiques.

Inclusion Criteria:

  • Be male or female
  • Be aged 18-60
  • Anyone who has been experiencing issues regarding at least two of the following for the past month: stomach discomfort, constipation, diarrhea, heartburn, bloating, gas, or abdominal pain
  • If taking any other supplements or herbal remedies that target gut or digestive health, has been doing so consistently for at least three months and is willing to maintain this for the duration of the study
  • Anyone willing to avoid introducing any other new supplements, medications, or herbal remedies for the duration of this trial
  • Anyone willing to maintain their current diet, sleep pattern, and activity levels for the duration of the trial
  • Anyone in good general health
  • Resides in the United States

Exclusion Criteria:

  • Anyone with a known history of severe digestive disorders like acid reflux, Irritable Bowel Syndrome (IBS), Irritable Bowel Disease (IBD), Crohn's disease, or gastrointestinal tract surgeries
  • Anyone with any known allergies or hypersensitivities to any supplement product ingredients
  • Anyone with a pineapple allergy
  • Anyone with any chronic health conditions that could impact participation in this study, such as cancer, mental health disorders, history of serious illness in the last three months, history of substance abuse, or planned surgery during the study period
  • Any women who are pregnant, breastfeeding, or trying to conceive (or who will be at any point during the study period)
  • Anyone currently taking prescription anticoagulants ('blood thinners') or with a history of a bleeding disorder
  • Anyone unwilling to follow the study protocol
  • Currently partaking in another research study or will be partaking in any other research study at any point during this study's duration
Entiende la evaluación inicial

Tratamiento, grupos y participación

El registro puede describir tratamientos y duración sin incluir un calendario completo. Pide al equipo las visitas, procedimientos, riesgos, costos y alternativas. Mantén tu atención habitual salvo que tu médico te indique un cambio.

Asignación
No aplica
Enmascaramiento
Sin enmascaramiento
Probiotics, Fibruline® Inulin Powder

No informado en este registro.

Dietary Supplement: Intervention Probiotics, Fibruline® Inulin Powder

Intervention Probiotics, Fibruline® Inulin Powder DIETARY_SUPPLEMENT

All participants will use the test product. Participants will answer questionnaires at Baseline, Week 4, Week 8, and Week 12.

Prepara tus preguntas

Qué evalúan los investigadores

Estas medidas indican qué se estudia. No prueban que un tratamiento funcione.

Medidas principales

Change in Gut Health (GSRS)

Plazo: Baseline, Week 4, Week 8, and Week 12

Change in gut health assessed via self-reported questionnaires including the Gastrointestinal Symptom Rating Scale (GSRS)

Change in Gut Health (Bristol Stool Scale)

Plazo: Baseline, Week 4, Week 8, and Week 12

Change in gut health assessed via self-reported questionnaires including the Bristol Stool Scale

Medidas secundarias

Change in Self-Reported Bloating

Plazo: Baseline, Week 4, Week 8, and Week 12

Assessed via self-reported questionnaire measuring participants' perceptions of the product's effects on bloating

Change in Self-Reported Digestive Comfort

Plazo: Baseline, Week 4, Week 8, and Week 12

Assessed via self-reported questionnaire measuring participants' perceptions of the product's effects on digestive comfort

Change in Self-Reported Regularity of Bowel Movements

Plazo: Baseline, Week 4, Week 8, and Week 12

Assessed via self-reported questionnaire measuring participants' perceptions of the product's effects on regularity of bowel movements

Change in Self-Reported Gasiness

Plazo: Baseline, Week 4, Week 8, and Week 12

Assessed via self-reported questionnaire measuring participants' perceptions of the product's effects on gasiness

Change in Self-Reported General Well-Being

Plazo: Baseline, Week 4, Week 8, and Week 12

Assessed via self-reported questionnaire measuring participants' perceptions of the product's effects on general well-being

El registro no indica resultados publicados.

Revisa las tablas completas y sus limitaciones en el registro oficial.

Abrir resultados oficiales ↗

Centros de investigación (1)

El estado general puede diferir del estado de un centro. Confirma la disponibilidad antes de trasladarte.

1 centros

CitruslabsLas Vegas, Nevada, United StatesReclutando

Equipo y fechas

Patrocinador principal
Peach Perfect
Inicio del estudio
1 feb 2026 Real
Finalización primaria
1 nov 2026 Estimado
Finalización del estudio
1 nov 2026 Estimado
Primera publicación
10 nov 2026 Real
Última actualización
10 nov 2026 Real

Contactos oficiales del estudio

Título oficial del estudio

A Clinical Trial to Evaluate the Effects of a Supplement on Gut Health

EL PRÓXIMO PASO, CON APOYO HUMANO

Consulta a Wellness Clinical Research

Tu mensaje va a WCR, incluso si otra organización realiza este estudio. WCR puede orientarte, pero podría no realizar este estudio, tener acceso a su equipo ni poder inscribirte.

No incluyas expedientes médicos, diagnósticos, medicamentos, números de seguro ni otros datos sensibles. Este formulario es para preguntas generales, no para atención urgente.

Enviar una pregunta no te inscribe en un estudio.

Fuente: API v2 de ClinicalTrials.gov. Patrocinadores e investigadores envían la información. La NLM no aprueba la seguridad ni la ciencia de todos los estudios registrados. Aviso del registro.

Consultado: 12 nov 2026 · Última actualización del registro: 10 nov 2026