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Hernia surgery fatigue? lidocaine may help you recover faster

NCT ID NCT07612839

Symptom relief Sponsor: Hakan Emirkadı Source: ClinicalTrials.gov ↗

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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 27, 2026 · Last updated Sep 04, 2026 · Updated 1 time

Summary

This study looks at whether giving a numbing medicine called lidocaine through a vein can help reduce tiredness after hernia repair surgery. About 80 adults having laparoscopic hernia repair will be randomly assigned to receive either lidocaine or standard care. Researchers will check fatigue, pain, nausea, and recovery for five days after surgery.

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.

Expected to start

Sep 2026

An estimate. Start dates often move.

Expected to finish

Jan 2027

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 to 65 years

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: * Age 18 to 65 years * Scheduled for elective laparoscopic transabdominal preperitoneal (TAPP) inguinal hernia repair * American Society of Anesthesiologists (ASA) physical status I or II * Able to understand and complete the Multidimensional Fatigue Inventory-20 (MFI-20) * Written informed consent provided Exclusion Criteria: * Known allergy or hypersensitivity to lidocaine or other amide-type local anesthetics * Clinically significant hepatic or renal dysfunction * Clinically significant cardiac rhythm or conduction disorder * Chronic opioid use * Regular use of antiarrhythmic medication * Pregnancy or breastfeeding * Planned use of an additional local anesthetic technique during the study intervention * Inability to complete the study assessments

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As listed by the trial registrant

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

Inguinal hernia unilateral Postoperative fatigue syndrome

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

  • University of Health Sciences Sultan Abdulhamid Han Training and Research Hospital

    Istanbul, Istanbul, 34668, Turkey (Türkiye)

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