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Can your pain threshold predict anesthesia needs during IVF?

NCT ID NCT07262216

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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

Summary

This study explores whether a woman's pain threshold, measured before the procedure, can predict how much anesthesia she will need during egg retrieval for IVF. Researchers will measure pain thresholds in 30 women and track the amount of sedatives they use. The goal is to personalize anesthesia to reduce drug exposure and improve safety and comfort.

What this could mean

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

Active substance
midazolam, propofol, fentanyl
What this could lead to
If successful, this could help doctors personalize anesthesia doses during egg retrieval, potentially reducing drug exposure and improving IVF outcomes.
What could go wrong
This is a small, early-stage observational study with only 30 participants. It does not test a new treatment, so results may not change practice directly.

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 30 people

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

Started

Apr 2025

Expected to finish

Dec 2025

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

Women who applied to the IVF center for treatment and agreed to participate in the study

Ages

18 to 50 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: * Women receiving IVF treatment Exclusion Criteria: * Dyspareunia history * Psychiatric disease * Vaginismus * ASA 3 patients

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Conditions

The condition(s) this trial relates to.

infertility disorder

As listed by the trial registrant

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

Conscious sedation Oocyte retrieval Pain threshold

Contacts and locations

Locations

  • Erciyes üniversitesi tıp fakültesi hastanesi

    Kayseri, Turkey (Türkiye)

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