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Kitchen staple may protect skin during surgery: paraffin oil tested against tourniquet burns

NCT ID NCT07523958

Prevention Sponsor: Istanbul Medipol University Hospital Source: ClinicalTrials.gov ↗

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 27, 2026 · Last updated Jun 27, 2026

Summary

This study tests whether applying paraffin oil to the skin before using a tourniquet (a tight band that stops blood flow) during arm surgery can prevent skin injuries like redness, blisters, or burns. About 90 adults having elective upper arm surgery will be randomly assigned to get either standard care or standard care plus paraffin oil. Researchers will check the skin right after the tourniquet is removed and again at 30 and 60 minutes later.

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 90 people

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

Started

Jan 2026

Expected to finish

Jul 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.

IInclusion Criteria: * Age ≥18 years * Patients scheduled for elective upper extremity surgery requiring pneumatic tourniquet application * ASA physical status I-III * Body mass index (BMI) \<30 kg/m² * Ability to provide informed consent * Willingness to participate in the study Exclusion Criteria: * Age \<18 years * Known dermatological disease or existing skin lesion at the tourniquet application site * Allergy or sensitivity to paraffin oil or related substances * Severe systemic disease (ASA IV or higher) * Obesity (BMI ≥30 kg/m²) * Emergency surgery * Patients transferred to intensive care postoperatively * Development of major postoperative complications (e.g., hematoma, seroma, nerve injury, significant bleeding) * Inability to communicate or comply with study procedures * Withdrawal from the study at any time

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Conditions

The condition(s) this trial relates to.

decubitus ulcer injury

As listed by the trial registrant

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

Pressure injury Skin injury Skin lesions

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

  • Kartal Dr. Lütfi Kırdar City Hospital Istanbul, Turkey

    RECRUITING

    Istanbul, 34760, Turkey (Türkiye)

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