Shock therapy for surgery pain? TENS device tested after gallbladder removal
NCT ID NCT05962853
First seen Jun 25, 2026 · Last updated Jun 26, 2026 · Updated 2 times
Summary
This study tested whether a TENS device (which sends mild electrical pulses through the skin) can help people recover after laparoscopic gallbladder removal. 140 adults were randomly assigned to receive TENS or standard care in the first 24 hours after surgery. Researchers measured pain levels and patient satisfaction to see if TENS improves outcomes.
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)
- What this could lead to
- If it works, this could offer a drug-free way to manage pain after gallbladder surgery, reducing the need for opioids.
- What could go wrong
- This is a small, completed study with no phase designation, so results may not apply broadly. TENS may not work for everyone and could cause skin irritation.
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
-
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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140 people
The number who actually took part.
- Started
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Jun 2023
- Finished
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Jun 2024
- 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 years and older
- 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.
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.
Inclusion Criteria: * Over 18 years old, * Without pacemaker and arrhythmia, * No previous history of chronic pain, alcohol or drug addiction, * Not using TENS/opioids before surgery, * Epidural analgesia is not applied in the postoperative period, without cognitive impairment, * No thoracic incision other than cholecystectomy, * Having at least 1 drain * No metastatic disease * No need for mechanical ventilation * As a result of the evaluation by the physician, there is no objection to the application of TENS, * Who agree to participate in the study, * No postoperative complications * Patients with American Society of Anesthesiology (ASA) evaluation I, II, III will be included in the sample group. Exclusion Criteria: * refuse to participate in the study
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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
-
Adana City Training and Research Hospital
Adana, Yüreğir / Adana, 01220, Turkey (Türkiye)
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Other studies related to the condition(s) this trial covers.
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