Completado

Trial of Encapsulated Ginger as a Treatment for Chemotherapy-Induced Nausea and Vomiting

0 criterios cumplidosConsulta de un vistazo cómo tu perfil cumple con cada criterio de elegibilidad.
Qué se está evaluando

Colección de datos

Quiénes están siendo reclutados

Náusea+2

+ Signos y Síntomas

+ Signos y Síntomas Digestivos

A partir de 18 años
Ver todos los criterios de elegibilidad
Cómo está diseñado el estudio

Estudio de Tratamiento

Fase 2
Intervencional
Inicio del estudio: junio de 2003
Ver detalles del protocolo

Resumen

Patrocinador PrincipalNational Center for Complementary and Integrative Health (NCCIH)
Última actualización: 27 de enero de 2026
Extraido de una base de datos validada por el gobierno.Reclamar como socio

Fecha de inicio: 1 de junio de 2003

Fecha en la que se inscribió al primer participante.

Chemotherapy induced nausea and vomiting significantly reduces patients' quality of life, increases fatigue, anxiety, and increases costs of health care delivery. Ginger (Zingiber officinalis) is already used in traditional folk medicine to treat nausea and vomiting in various populations. Ginger's ability to block 5-HT3 receptors and its free-radical scavenging in the intestines suggest that it may be beneficial for reducing both the prevalence and severity of chemotherapy induced nausea and vomiting. Despite ginger's possible benefits in reducing the prevalence and severity of chemotherapy induced nausea and vomiting, no dosing and/or safety studies have been performed. This study will assess the efficacy and safety of two dose levels (1000 mg, or 2000 mg, orally/day) of Zingiber officinalis extract (standardized for 5% gingerols) in patients undergoing chemotherapy (cisplastin or adriamycin) who have experienced at least one episode of chemotherapy induced nausea and vomiting despite optimal conventional medical therapy. The primary aim of the study is to determine the most efficacious dose of powdered ginger-root for reducing the prevalence and severity of acute nausea and vomiting. Secondary aims of the study include (1) determination of the most efficacious dose of powdered ginger-root for reducing the prevalence and severity of delayed nausea and vomiting; (2) assessment of the safety of different doses of oral powdered ginger root in patients receiving chemotherapy; and (3) determination if study participants can discern if they are receiving placebo or ginger. Participants receiving either adriamycin or cisplatin for cancer related treatment will be randomized to receive one of two doses of powdered ginger or placebo immediately prior to chemotherapy infusion. Participants will be followed for 72 hours after infusion in order to assess frequency and severity of nausea and vomiting. Baseline and 72 hour post chemotherapy labs will be used to assess safety profile of ginger.

Título OficialTrial of Encapsulated Ginger as a Treatment for Chemotherapy-Induced Nausea and Vomiting
Patrocinador PrincipalNational Center for Complementary and Integrative Health (NCCIH)
Última actualización: 27 de enero de 2026
Extraido de una base de datos validada por el gobierno.Reclamar como socio

Protocolo

Esta sección proporciona detalles del plan del estudio, incluyendo cómo está diseñado y qué se está evaluando.
Detalles del Diseño

Se reclutarán 180 pacientes

Número total de participantes que el ensayo clínico espera reclutar.

Estudio de Tratamiento

Estos estudios prueban nuevas formas de tratar una enfermedad, condición o problema de salud. El objetivo es determinar si un nuevo medicamento, terapia o enfoque funciona mejor o tiene menos efectos secundarios que las opciones existentes.


Elegibilidad

Los investigadores buscan pacientes que cumplan ciertos criterios, conocidos como criterios de elegibilidad: estado general de salud o tratamientos previos.
Condiciones
Criterios

Cualquier sexo

Sexo biológico de los participantes elegibles para inscribirse.

A partir de 18 años

Rango de edades de los participantes que pueden unirse al estudio.

Voluntarios sanos no permitidos

Indica si personas sanas, sin la condición que se estudia, pueden participar.

Condiciones

Patología

NáuseaSignos y SíntomasSignos y Síntomas DigestivosCondiciones Patológicas, Signos y SíntomasVómito

Criterios

Inclusion criteria: * Confirmed diagnosis of cancer and currently receiving chemotherapy * Currently being treated with any chemotherapeutic agent at any dose, and have experienced nausea and/or vomiting from a previous round of chemothearpy * Scheduled to receive a 5-HT3 receptor antagonist antiemetic: ondansetron (Zofran®) granistron (Kytril®), tropisetron (Navoban®) or dolasetron mesylate (Anzemet®), palanosetron (Alozi) and/or the NK1 antagonist aprepitant (Emend) * Must be able to swallow capsules * Must be able to understand English or Spanish, complete questionnaires in English or Spanish * Women of childbearing age to use appropriate birth control Exclusion criteria: * Chemotherapy regimens with multiple-day doses * Clinical evidence of current or impending bowel obstruction or symptomatic brain metastases * Concurrent radiotherapy that is classified as high or intermediate risk of causing nausea and vomiting; total body irradiation, hemi-body, upper abdomen, abdominal-pelvic mantle, cranium, craniospinal irradiation * Pregnant or lactating * Patients with a history of a bleeding disorder(s) or those experiencing thrombocytopenia * Currently be taking ginger or have taken ginger in the last month * Have an allergy to ginger

Centros del Estudio

Estos son los hospitales, clínicas o centros de investigación donde se lleva a cabo el estudio. Puedes encontrar la ubicación más cercana a ti y su estado de reclutamiento.

Este estudio tiene 6 ubicaciones

Suspendido

Northern Indiana Cancer Research Consortium CCOP

South Bend, United StatesAbrir Northern Indiana Cancer Research Consortium CCOP en Google Maps
Suspendido

University of Michigan Cancer Center Complementary and Alternative Medicine Research Center

Ann Arbor, United States
Suspendido

St. Joseph Mercy Hospital

Ann Arbor, United States
Suspendido

Community Clinic Oncology Program

Grand Rapids, United States
Completado6 Centros de Estudio