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Shock therapy for surgery pain? TENS device tested after gallbladder removal

NCT ID NCT05962853

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

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

140 people

The number who actually took part.

Started

Jun 2023

Finished

Jun 2024

Lead sponsor

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

18 years and older

Sex

Anyone

Healthy volunteers

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

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.