Clinical Trials Directory

Trials / Completed

CompletedNCT04378998

Is Acupuncture Able to Reduce Nausea and Vomiting in the Terminal Ill Patient

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
136 (actual)
Sponsor
University of Aarhus · Academic / Other
Sex
All
Age
Healthy volunteers
Not accepted

Summary

A comparative effectiveness research design was used. The sample size was calculated to 136 patients, who were randomized to an intervention group and a control group respectively. The patients were terminal ill patients enrolled to three in-bed hospices in Denmark and nausea and vomiting were measured using EORTC QlQ-c15-PAL (European Organisation for Research and Treatment of Cancer, Quality of Life Questionaire, core 15, Palliation)

Detailed description

The terminal ill patient is suffering from many different symptoms. In total 70% are suffering from nausea and vomiting due to the wide spread of cancer or due to side effects of treatment. Often the antiemetic's are not able to reduce symptoms to a level that enable the patient to experience quality in life in the last days of his life. The investigators had some experience with acupuncture as a complementary therapy but the investigators wanted more systematically to investigate if acupuncture is able to reduce the terminal ill patient´s nausea and vomiting. Literature show that acupuncture is able to reduce nausea and vomiting in patients receiving chemotherapy, but there is no literature that support the ability of acupuncture to reduce nausea and vomiting in the terminal ill patient. The purpose of this study was to generate evidence based knowledge close to practice regarding the effect of acupuncture in reducing nausea and vomiting in the terminal ill patient. Participants: Terminal ill patients suffering from nausea and/or vomiting Interventions: The intervention group received usual care plus acupuncture for three days. The acupuncture spots: Pericardium-6, Stomach-36, Liver-3 and Yin Tang were used. The control group received usual care.

Conditions

Interventions

TypeNameDescription
OTHERAcupunctureThe intervention group received usual care plus acupuncture for three days. The acupuncture spots: Pericardium-6, Stomach-36, Liver-3 and Yin Tang were used. The control group received usual care.

Timeline

Start date
2015-01-25
Primary completion
2019-10-25
Completion
2019-10-25
First posted
2020-05-07
Last updated
2020-05-07

Source: ClinicalTrials.gov record NCT04378998. Inclusion in this directory is not an endorsement.