Phase
Condition
Colic
Stomach Discomfort
Lactose Intolerance
Treatment
N/AClinical Study ID
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Have a diagnosis of advanced cancer with an estimated prognosis of less than 1 yearbut more than 3 days.
Describe their nausea as at least moderate on a Likert scale OR at have had at leastone vomit per day for the last three days.
Have an underlying cause for their nausea which is thought to be irreversible OR thepatient has made an autonomous choice not to proceed with treatment for anypotentially reversible cause (for example surgery for obstruction or drainage ofascites).
Can be male or female patients but must be over the age of 18.
Have signed a consent form prior to entering the study.
If patients are taking corticosteroids the dosage should be stable for 3 days beforeand during the trial.
Be thought to be well enough to complete the 3 day trial.
Exclusion
Exclusion criteria:
Arm lymphoedema.
Weakness, fatigue or confusion sufficient that patient is unable to take part.
Previous history of acupuncture/acupressure for nausea or vomiting, or history of useof acupressure by a close relative.
History of Parkinsonism or Parkinsonism on examination.
Patients will not be enrolled if they are sharing a room with another patient takingpart in the study.
Patients who are unable to read or comprehend the questionnaire or Visual AnalogueScale.
Study Design
Study Description
Connect with a study center
Sue Ryder Care Leckhampton Court Hospice
Cheltenham, Gloucestershire GL53 0QJ
United KingdomActive - Recruiting
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