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New rehab combo aims to fix wobbly breastbone after heart surgery

NCT ID NCT07381387

Symptom relief Sponsor: Beni-Suef University 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jun 27, 2026

Summary

This study looks at whether adding LASER therapy and specific abdominal exercises to standard rehab can improve breastbone healing after open-heart surgery. 120 adults with an unstable breastbone will be split into four groups to compare different exercise and LASER combinations. The goal is to reduce pain and movement at the surgical site, helping people recover better.

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 120 people

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

Expected to start

Jan 2026

An estimate. Start dates often move.

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 : All included patients will be: * Their age 18\<. * Both sexes. * Hemodynamic stable. * Acute sternal instability. * Able to provide informed consent. Exclusion criteria: Patient will be excluded if: * Emergency or urgent operation. * Revision sternotomy. * Manifesting hypoxemia. * Partial oxygen pressure in arterial blood \< 60 mmHg. * Renal insufficiency with serum creatinine ≥ 1. 8 mg/dl after surgery. * Low cardiac output syndrome with ST segment elevation in multiple electrocardiogram leads. * Cardiac arrhythmias or hypotension. * Other medical conditions, such as diabetes, uncontrolled hypertension and obesity. * Previous medical history including conditions that may have influenced the provision of physiotherapy interventions, such as severe asthma, chronic airflow limitation, bronchiectasis, ankylosing spondylitis or lumbar disc prolapse. * Impaired cognition.

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As listed by the trial registrant

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

Sternal instability after median sternotomy

How to take part

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

  1. The study's own enquiry address

    This study publishes an address for enquiries. See it below .

  2. The places running it

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

  3. 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 ↗

  4. A doctor treating you

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Contacts and locations

Locations

  • مستشفي القلب الحامعي -مستشفيات جامعه اسيوط

    Asyut, Egypt

    Contact Email: •••••@•••••