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Which anesthesia is best for a common gynecological procedure? new study investigates

NCT ID NCT07358624

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
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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study compared spinal anesthesia to general anesthesia in 84 women undergoing diagnostic hysteroscopy, a procedure to look inside the uterus. Researchers measured pain levels and patient satisfaction after the procedure. The goal was to find which method causes less discomfort and leads to a better experience.

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 one method proves better, it could help doctors choose the best anesthesia for women having this common procedure, improving comfort and recovery.
What could go wrong
This is a small, single-center study with only 84 participants. Results may not apply to all patients or settings, and the study is already completed without a clear winner yet.

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

84 people

The number who actually took part.

Started

Sep 2024

Finished

Jan 2025

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 to 90 years

Sex

Female participants only

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: * written informed consent. * an American Society of Anesthesiologists (ASA) physical status of I, II, or stable III in * women scheduled for diagnostic hysteroscopy Exclusion Criteria: * operative hysteroscopy. * contraindications to spinal anesthesia. * known allergy to anesthetic agents. * full stomach. * body mass index \>35 kg/m². * history of migraine. * communication difficulties Patients were excluded from the final analysis in case of: * spinal anesthesia failure requiring conversion to general anesthesia. * failure of ventilation with a supraglottic airway requiring tracheal intubation. * conversion to laparotomy. * prolonged hospitalization for non-anesthesia-related complications. * loss to follow-up after discharge.

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Conditions

The condition(s) this trial relates to.

Pain, Postoperative Patient Satisfaction

As listed by the trial registrant

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

Contacts and locations

Locations

  • Charles Nicolle hospital Tunis

    Bab Saadoun, Tunis, 1006, Tunisia

More trials for these conditions

Other studies related to the condition(s) this trial covers.