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Which nose surgery method is safer for your heart?

NCT ID NCT07425834

Knowledge-focused Sponsor: Fatmaelzahraa Omar Mahmoud Bahr Source: ClinicalTrials.gov ↗

What the study statuses mean

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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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 compares two techniques used during septoplasty (nose surgery to fix a deviated septum): cold dissection and electrocautery. The goal is to see which method causes fewer sudden drops in heart rate during the operation. 120 adults aged 18-60 who need this surgery will be randomly assigned to one of the two techniques, and their heart rates will be closely monitored.

What this could mean

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

What this could lead to
If this trial succeeds, it could help surgeons choose a safer technique for septoplasty, reducing the risk of heart rate drops during surgery.
What could go wrong
This is a small, early-stage study that only looks at a temporary side effect during surgery. The results may not apply to all patients or change standard practice.

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.

Participants

About 120 people

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

Expected to start

May 2026

An estimate. Start dates often move.

Expected to finish

Mar 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.

Who is studied

Randomization and Group Allocation Patients will be randomly allocated into two groups using computer-generated randomization:

Ages

18 to 60 years

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

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 18-60 years. * Indicated for primary septoplasty. * American Society of Anesthesiologists (ASA) physical status I-II. Exclusion Criteria: * History of cardiac arrhythmias or conduction abnormalities. * Use of beta-blockers, calcium channel blockers, or antiarrhythmic drugs Previous nasal surgery. * Combined nasal procedures. * Intraoperative complications requiring deviation from the assigned technique.

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As listed by the trial registrant

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

Septoplasty surgeries

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

  • Fayoum University Hospital

    Al Fayyum, 63514, Egypt

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