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Does anesthesia choice affect clotting in prostate surgery? a trial investigates

NCT ID NCT07734233

Knowledge-focused Sponsor: Haseki Training and Research 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jul 29, 2026 · Last updated Jul 30, 2026 · Updated 1 time

Summary

This trial compares spinal anesthesia (using bupivacaine) with general anesthesia in men undergoing transurethral resection of the prostate (TURP) for benign prostatic hyperplasia. Researchers measure blood clotting and breakdown markers before surgery and at 1 and 24 hours after, to see if the type of anesthesia influences coagulation and fibrinolysis. The study also tracks blood pressure, heart rate, and complications during and after surgery.

What this could mean

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

Active substance
Spinal anesthesia (bupivacaine) or general anesthesia (propofol, fentanyl, rocuronium, sevoflurane)
What this could lead to
If one anesthesia method proves safer for blood clotting, it could guide choices for prostate surgery patients.
What could go wrong
This is a small, early-stage study focused on lab tests, not clinical outcomes. Results may not change practice.

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

78 people

The number who actually took part.

Started

Oct 2024

Finished

Mar 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 years and older

Sex

Male 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: * Male patients * Age ≥18 years * Scheduled for elective bipolar transurethral resection of the prostate * ASA physical status I-II * Ability to provide written informed consent Exclusion Criteria: * History of deep vein thrombosis or pulmonary embolism * Known inherited or acquired coagulation disorder * Severe hepatic insufficiency * Severe renal insufficiency * Use of anticoagulants, antiplatelet drugs, or NSAIDs within 10 days before surgery * Platelet count \<100 × 10⁹/L * INR \>1.5 * aPTT \>47 seconds * Contraindications to spinal anesthesia * Prostate malignancy * ASA physical status III or higher * Refusal to participate

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Conditions

The condition(s) this trial relates to.

benign prostatic hyperplasia thrombotic disease

As listed by the trial registrant

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

Benign prostatic hyperplasia Transurethral resection of the prostate (TURP)

Contacts and locations

Locations

  • Sultangazi Haseki Training and Research Hospital

    Istanbul, Istanbul, 34265, Turkey (Türkiye)

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