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Preemptive pain meds cut opioid need after hysterectomy

NCT ID NCT07401927

Symptom relief Sponsor: Giresun 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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 looked at whether giving ibuprofen and paracetamol before laparoscopic hysterectomy surgery helps control pain afterward. 70 adults participated. Researchers measured pain scores, opioid use, and side effects like nausea during the first 24 hours after surgery.

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

70 people

The number who actually took part.

Started

Feb 2026

Finished

May 2026

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

Female patients aged 18 to 70 who are scheduled to undergo laparoscopic hysterectomy surgery.

Ages

18 to 70 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: * Aged 18-70 * ASA I-III patients * Patients undergoing elective laparoscopic hysterectomy surgery Exclusion Criteria: * Emergency surgery * Patients who require conversion to abdominal hysterectomy during the intraoperative period * Those with severe liver or kidney failure, a history of long-term nonsteroidal anti-inflammatory and opioid analgesic use * Those with a history of gastrointestinal bleeding, peptic ulcer or inflammatory bowel disease, diabetes or other neuropathic diseases * Patients unable to use patient-controlled analgesia (PCA) devices

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As listed by the trial registrant

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

Laparoscopic hysterectomy Postoperative analgesia

Contacts and locations

Locations

  • Operating Room at the Giresun Obstetrics and Gynecology and Pediatrics Training and Research Hospital

    Giresun, Turkey (Türkiye)

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