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Nerve block eases Post-Surgery insomnia and anxiety in women

NCT ID NCT07384468

Symptom relief Sponsor: Xiaochen Ji 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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 27, 2026 · Last updated Jun 27, 2026

Summary

This study tested whether a nerve block (stellate ganglion block) combined with standard anesthesia could help women with uterine fibroids sleep better and feel less anxious after laparoscopic surgery. 233 women aged 35-55 took part. Results aim to show if this approach reduces stress, pain, and improves recovery.

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

233 people

The number who actually took part.

Started

May 2022

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

35 to 55 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: * Female patients aged 35 to 55 years. * Diagnosed with uterine fibroids and scheduled for elective laparoscopic myomectomy. * American Society of Anesthesiologists (ASA) physical status classification I or II. * Normal cognitive function and ability to understand the study procedures. * Provided written informed consent prior to participation. Exclusion Criteria: * Contraindications to stellate ganglion block, including coagulation disorders, infection at the puncture site, or allergy to local anesthetics. * Severe dysfunction of major organs, including heart, liver, or kidney. * Poorly controlled chronic diseases such as hypertension or diabetes mellitus. * History of psychiatric disorders, chronic pain conditions, or long-term use of sedatives, analgesics, or medications affecting autonomic nervous system function. * Preexisting significant sleep disorders prior to surgery. * Abnormal cervical anatomy, history of cervical surgery, or radiotherapy. * Anticipated difficult airway. * Conversion to open surgery during the procedure. * Failure of stellate ganglion block. * Occurrence of serious adverse events related to the block procedure, such as nerve injury, arrhythmia, or local anesthetic systemic toxicity. * Unplanned admission to the intensive care unit after surgery.

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Conditions

The condition(s) this trial relates to.

leiomyoma Pain, Postoperative uterine corpus leiomyoma

As listed by the trial registrant

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

Uterine fibroids (UF)

Contacts and locations

Locations

  • Cangzhou Central Hospital

    Cangzhou, Hebei, 061001, China

More trials for these conditions

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