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New hospital gown aims to give surgery patients privacy and comfort

NCT ID NCT07607457

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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

Summary

This study will test a specially designed patient gown for people recovering from abdominal surgery. The gown aims to be more private, comfortable, and easier to move in than standard hospital gowns, while also allowing doctors and nurses easy access to medical devices like drains and catheters. About 172 patients and 14 healthcare workers will take part to see if the new design improves satisfaction and care.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
enhanced patient gown
What this could lead to
If this gown works well, it could become a new standard for hospital wear, making recovery more comfortable and dignified for surgery patients.
What could go wrong
This is a small, early-stage trial testing a prototype. The gown may not prove significantly better than current options, and results may not apply to all hospitals or surgeries.

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 172 people

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

Expected to start

Jun 2026

An estimate. Start dates often move.

Expected to finish

Dec 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.

Patient Inclusion Criteria for the Study: * Be 18 years of age or older * Have undergone major abdominal surgery performed on an elective basis in a general surgery clinic (e.g., colorectal surgery, gastric surgery, hepatobiliary surgery, etc.) * Currently receiving care and treatment with medical devices (e.g., drains, Foley catheters, etc.) * Willing to participate in the study Patient Inclusion Criteria for the Study: * The participant refuses to wear a hospital gown * The participant has an allergy to the specified fabric Patients who are unable to mobilize for any reason (paralysis, general health impairment, history of stroke, etc.) * Patients with difficulty speaking and understanding Turkish * Patients lacking cognitive competence * Patients who develop complications within the first 24 hours after surgery and require revision surgery * Patients with prolonged intensive care unit (ICU) stays during the postoperative period * Since both the standard-sized traditional patient gown and the newly developed patient gown (available in sizes M-L) will be used in the study, patients whose body measurements do not fit within this size range will not be included in the study. This approach was adopted to prevent differences in comfort, mobility, and safety resulting from size mismatch from influencing the results, to ensure standardization in measurements, and to maintain comparability between the intervention and control groups. Inclusion Criteria for Healthcare Professionals in the Study: * Providing care to patients who have undergone abdominal surgery * Having worked in the field for more than one year * Volunteering to participate in the study Exclusion Criteria for Healthcare Professionals in the Study: • Being on leave or on sick leave during the study period.

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As listed by the trial registrant

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How to take part

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  1. The official record

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