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Prevention of Postoperative Nausea and Vomiting (PONV) by Acupressure

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00275483
First Posted: January 12, 2006
Last Update Posted: May 28, 2008
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
Herlev Hospital
January 10, 2006
January 12, 2006
May 28, 2008
May 2005
October 2005   (Final data collection date for primary outcome measure)
Postoperative nausea and vomiting
Same as current
Complete list of historical versions of study NCT00275483 on ClinicalTrials.gov Archive Site
  • 1: The use of conventionel antiemetic treatment.
  • 2: Lenght of stay in the perioperative unit.
  • 3: overall lenght of stay
Same as current
Not Provided
Not Provided
 
Prevention of Postoperative Nausea and Vomiting (PONV) by Acupressure
Prevention of PONV by Acupressure. A Study of the Effect of a Recently Generated Danish Bracelet Vital-Band(R) Which Stimulates the Acupressure Point P6
The purpose of this study is to determine whether stimulation to the akupressurpoint P6 with a recently developed bracelet are effective preventing postoperative nausea and vomiting
Not Provided
Interventional
Phase 4
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Triple (Participant, Care Provider, Outcomes Assessor)
Primary Purpose: Prevention
  • Postoperative Nausea and Vomiting
  • Acupressure Point P6
Device: Vital-band (R)
Not Provided
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
132
February 2007
October 2005   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  • Female,
  • Non-smoker,
  • >18 years,
  • ASA 1 or 2,
  • Signed patient information,
  • IV-anaestesia.

Exclusion Criteria:

  • Male,
  • Smoker,
  • ASA 3 or 4,
  • Pregnancy,
  • Nausea and vomiting within the last 24 h before operation,
  • Diabetes,
  • Carpaltunnel syndrome,
  • Lymphedema of arms,
  • Eczema of forearm,
  • Patients who earlier has undergone removal of lymph nodes in the armpits,
  • Inhalation anaestesia.
Sexes Eligible for Study: Female
18 Years and older   (Adult, Senior)
No
Contact information is only displayed when the study is recruiting subjects
Denmark
 
 
NCT00275483
Vital-band 01
Not Provided
Not Provided
Not Provided
Not Provided
Herlev Hospital
Not Provided
Principal Investigator: Birgitte Majholm, MD Herlev Hospital
Herlev Hospital
May 2008

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP