Last updated: January 8, 2021
Sponsor: University Medicine Greifswald
Overall Status: Active - Recruiting
Phase
N/A
Condition
N/ATreatment
N/AClinical Study ID
NCT03821428
BB 166/18
Ages 30-65 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Patients with an American Society of Anesthesiologists physical status of I to IIIscheduled for elective ambulatory transesophageal echocardiography (TEE) withoutsedation
- TEE time does not exceed 30 minutes
- Patients without previous opioid and psychotropic medication
- Patients aged between 30 and 65 years, able to use visual analogue scale 100 mm
- Patients who have given written informed consent
Exclusion
Exclusion Criteria:
- Current psychiatric disease
- Local skin infection at the sites of acupuncture
- Aged < 30 or > 65 years
- TEE time more than 30 min
- Patients who consumed opioid medication at least 6 months before surgery
- Patients with the history of: i) psychiatric disease; ii) insulin-dependent diabetesmellitus; iii) radio- or chemotherapy; iv) peripheral polyneuropathy.
- Patients who are unable to understand the consent form or to use visual analogue scale 100 mm
Study Design
Total Participants: 60
Study Start date:
January 13, 2019
Estimated Completion Date:
May 20, 2021
Study Description
Connect with a study center
University Medicine of Greifswald
Greifswald, 17475
GermanyActive - Recruiting
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