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Can exercise speed recovery after fibroid surgery?

NCT ID NCT07661147

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 compares aerobic exercises (like walking and cycling) with resistance exercises to see which better reduces disability and pain in women who have had an abdominal myomectomy. Participants are women aged 30 to 60, six to twelve months after surgery, with no complications except weak abdominal muscles. The goal is to find the best exercise approach to improve function and quality of life after this procedure.

What this could mean

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

Active substance
exercise (aerobic and resistance training)
What this could lead to
If effective, this could point toward a standard exercise program to help women recover faster and with less disability after myomectomy.
What could go wrong
This is a small, early-stage study with 60 participants, so results may not apply to all patients. Exercise programs require adherence, and individual responses vary.

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 60 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

Oct 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

30 to 60 years

Sex

Female participants only

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: * All patients are conscious and ambulant. * Their ages ranged from 30-60 years old. * All patients will be under post abdominal myomectomy (6-12 months) management program. * All patients will not suffer from any complication post abdominal myomectomy, except weakness of abdominal muscles. * All patients will receive and agreed to sign the informed consent form. Exclusion Criteria: * The patient who has cardiovascular diseases, or uncontrolled hypertension. * The patient who has cardiac pacemakers or other implanted electronic devices. * Uncooperative patients. * Patients who have cardiopulmonary diseases. * Patients who have psychic disorders. * Patients with neuromuscular diseases. * Pregnant female. * Patients who have any endocrine, metabolic, renal or hepatic diseases. Patients who have an open wound at or near the treatment site.

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As listed by the trial registrant

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

How to take part

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  1. The official record

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