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Zap away surgery jitters? TENS device tested for gallbladder op

NCT ID NCT07307703

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study tests whether a non-invasive device called TENS, which delivers mild electrical currents through the skin, can reduce anxiety and pain and improve satisfaction in 80 adults having laparoscopic gallbladder removal. Participants will receive either standard care or TENS before and after surgery. The goal is to see if this simple technique can make recovery 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) device
What this could lead to
If it works, this could offer a simple, drug-free way to ease anxiety and pain and improve satisfaction for people undergoing gallbladder surgery.
What could go wrong
This is a small, early-stage study with only 80 participants. The results may not apply to everyone, and TENS may not provide meaningful benefits over standard care.

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

About 80 people

The number the study aims to enrol. It can still change while the study runs.

Started

Dec 2025

Expected to finish

Sep 2026

An estimate. End dates often move.

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: * Adults aged 18-65 years scheduled for elective laparoscopic cholecystectomy ASA (American Society of Anesthesiologists) physical status classification I-II Ability to understand the study procedures and provide written informed consent No contraindications to TENS application (e.g., intact skin at electrode placement sites) Willingness to comply with perioperative assessments (pain, anxiety, satisfaction scales) Exclusion Criteria: * Patients with ASA III or higher physical status Presence of cardiac pacemaker or other implanted electrical devices History of epilepsy, severe neuropathy, or psychiatric disorders affecting pain/anxiety perception Skin lesions, infections, or dermatological conditions at electrode placement sites Use of analgesics, anxiolytics, or sedatives beyond standard perioperative protocols Emergency cholecystectomy or conversion to open surgery Pregnant or breastfeeding women Patients unwilling or unable to provide informed consent

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Conditions

The condition(s) this trial relates to.

cholelithiasis gallstones Pain, Postoperative

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • Adana City Hospital

    RECRUITING

    Niğde, Adana, 51100, Turkey (Türkiye)

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