Needle vs. gag: acupuncture may ease discomfort during heart test
NCT ID NCT03821428
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether acupuncture at specific points (CV24 and P6) can reduce gagging in 60 adults undergoing a transesophageal echocardiogram (a heart ultrasound done through the throat). Participants received either real or placebo acupuncture. The goal was to see if the treatment made the procedure more comfortable and reduced the need for rescue medication.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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60 people
The number who actually took part.
- Started
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Jan 2019
- Finished
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May 2021
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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30 to 65 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Patients with an American Society of Anesthesiologists physical status of I to III scheduled for elective ambulatory transesophageal echocardiography (TEE) without sedation 2. TEE time does not exceed 30 minutes 3. Patients without previous opioid and psychotropic medication 4. Patients aged between 30 and 65 years, able to use visual analogue scale 100 mm 5. Patients who have given written informed consent Exclusion Criteria: 1. Current psychiatric disease 2. Local skin infection at the sites of acupuncture 3. Aged \< 30 or \> 65 years 4. TEE time more than 30 min 5. Patients who consumed opioid medication at least 6 months before surgery 6. Patients with the history of: i) psychiatric disease; ii) insulin-dependent diabetes mellitus; iii) radio- or chemotherapy; iv) peripheral polyneuropathy. 7. Patients who are unable to understand the consent form or to use visual analogue scale 100 mm
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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University Medicine of Greifswald
Greifswald, 17475, Germany