ClinicalTrials.Veeva

Menu

Prevention of Postoperative Nausea and Vomiting (PONV) by Acupressure

H

Herlev Hospital

Status and phase

Completed
Phase 4

Conditions

Acupressure Point P6
Postoperative Nausea and Vomiting

Treatments

Device: Vital-band (R)

Study type

Interventional

Funder types

Other

Identifiers

NCT00275483
Vital-band 01

Details and patient eligibility

About

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

Enrollment

132 patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

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.

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems