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Estrogen levels linked to recovery after IVF procedure

NCT ID NCT06925633

Knowledge-focused Sponsor: Konya City Hospital 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 98 women undergoing IVF egg retrieval under general anesthesia. Researchers measured their estrogen levels before the procedure and then tracked how well they recovered over the next three days. The goal was to see if higher estrogen levels were linked to better or worse recovery, including pain, nausea, and overall well-being. Since this was an observational study, no treatment was given—it simply gathered information to guide future care.

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 the findings are clear, this could help doctors better predict and manage recovery for IVF patients.
What could go wrong
This is an observational study, not a treatment trial. It cannot prove cause and effect, and results may not apply to all patients.

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

98 people

The number who actually took part.

Started

Apr 2025

Finished

Dec 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.

Who is studied

The study population consists of adult female patients aged 18 to 45 years undergoing transvaginal oocyte retrieval under general anesthesia as part of an IVF procedure. All participants will have ASA physical status I or II and be able to provide informed consent.

Ages

18 to 45 years

Sex

Female participants only

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 between 18 and 45 years * ASA physical status I or II * Scheduled for transvaginal oocyte retrieval under general anesthesia as part of an IVF procedure * Willing and able to provide written informed consent * Able to understand and complete study questionnaires (QoR-15, HADS) Exclusion Criteria: * ASA physical status III or IV * History of severe renal, hepatic, respiratory, or cardiovascular disease * Current or chronic use of psychotropic medications * Chronic use of opioids or benzodiazepines * Known psychiatric or neurological disorders that may interfere with study participation * Inability to provide informed consent or complete study questionnaires

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As listed by the trial registrant

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

Anesthesia recovery period Estrogens In vitro fertilization Postoperative recovery

Contacts and locations

Locations

  • Konya City Hospital

    Konya, 42090, Turkey (Türkiye)

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