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Electric pulses on the wrist may tame colonoscopy pain
NCT ID NCT06813703
First seen Aug 14, 2026 · Last updated Aug 14, 2026
Summary
This trial tests whether a mild electrical stimulation device, applied near the wrist and ankle, can reduce pain during a colonoscopy performed without sedation. Sixty adults aged 18 to 75 will be randomly assigned to receive either real stimulation or a sham version. While the procedure happens, researchers will monitor brain activity using EEG and infrared sensors to see how the stimulation affects pain-related brain regions. The goal is to understand if this technique offers a safe, non-drug way to make unsedated colonoscopy more comfortable.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Transcutaneous electrical nerve stimulation (TENS) based on wrist-ankle acupuncture theory
- What this could lead to
- If it works, this could offer a drug-free way to reduce pain during colonoscopy without sedation, making the procedure more comfortable for patients.
- What could go wrong
- This is a small, early-stage trial, so results may not apply broadly. The sham control uses minimal stimulation, and pain relief may be modest or vary between individuals.
This is an AI summary of the original study and may miss details. Read our disclaimer.
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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Feb 2025
- Finished
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Mar 2026
- 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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18 to 75 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
1. Inclusion Criteria: * Patients undergoing unsedated colonoscopy are eligible for inclusion in this study. * Aged 18 to 75 years. * Meeting the requirements for colonoscopy, with good cardiopulmonary function and stable vital signs. * A pre-procedural Visual Analog Scale (VAS) pain score of less than 3. 2. Exclusion Criteria: * Participants with speech or cognitive impairments. * Those with acute anal or rectal stenosis, acute perianal or rectal infections, acute diverticulitis, or active inflammatory bowel disease. * Women who are menstruating, pregnant, or breastfeeding. * Patients with active tuberculosis, hemophilia, or advanced malignant tumors. * Individuals with sensory disturbances, implanted pacemakers or defibrillators, or ankle skin ulcers. * Those who have used sedatives or analgesics either long-term or within the past 24 hours. * Individuals with any condition that interferes with EEG-fNIRS signal acquisition, such as cranial abnormalities, implanted metal or electronic devices, epilepsy, or neurological disorders.
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Conditions
The condition(s) this trial relates to.
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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The First Affiliated Hospital of Naval Medical University
Shanghai, Shanghai Municipality, 200433, China
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