Preoperative Anxiety and Surgical Fear in Holmium Laser Enucleation of the Prostate and Transurethral Resection of the Prostate Patients With Benign Prostatic Hyperplasia

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexMale
Age50+
SponsorHitit University

About this trial

Benign prostatic hyperplasia (BPH) is a common condition in older men and may cause bothersome lower urinary tract symptoms that can negatively affect quality of life. Surgical treatment with Holmium Laser Enucleation of the Prostate (HoLEP) or Transurethral Resection of the Prostate (TURP) is often recommended when medical therapy is insufficient.

This prospective observational study aims to evaluate whether preoperative anxiety, depression, and surgical fear influence postoperative functional outcomes, urinary continence, erectile function, and patient satisfaction in patients undergoing HoLEP or TURP for BPH. Participants will complete validated psychological and functional questionnaires before surgery and during postoperative follow-up visits at 1 and 3 months. The study will also assess changes in psychological status after surgery and compare outcomes between HoLEP and TURP patients.

The findings may help improve preoperative patient counseling and identify patients who could benefit from additional psychological support before surgery.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Male patients aged 50 years or older

Diagnosis of benign prostatic hyperplasia (BPH)

Scheduled to undergo HoLEP or TURP

Ability to understand and complete study questionnaires

Disqualifiers

History of severe psychiatric disorder

Active psychiatric treatment

Neurogenic bladder or neurologic voiding dysfunction

Diagnosis of prostate cancer

Trial population

Male patients aged 50 years or older with benign prostatic hyperplasia (BPH) who are scheduled to undergo Holmium Laser Enucleation of the Prostate (HoLEP) or Transurethral Resection of the Prostate (TURP) at Hitit University Erol Olcok Training and Research Hospital and who provide written informed consent.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • Holmium Laser Enucleation of the Prostate (HoLEP)

    Procedure/Surgery

    Standard HoLEP procedure for treatment of benign prostatic hyperplasia.

  • Transurethral Resection of the Prostate (TURP)

    Procedure/Surgery

    Standard TURP procedure for treatment of benign prostatic hyperplasia.

Treatment groups

80 Participants
are divided into 2 treatment groups
Group A: HoLEP Group1 intervention
Group B: TURP Group1 intervention

Trial outcomes

Primary outcomes

1

Change in International Prostate Symptom Score (IPSS)

Association between preoperative anxiety levels and postoperative functional improvement measured by changes in International Prostate Symptom Score (IPSS). IPSS scores range from 0 to 35, with higher scores indicating more severe lower urinary tract symptoms. Change from baseline to postoperative 3 months will be evaluated.

Time frame
Baseline to 3 months after surgery

Secondary outcomes

1

Change in IIEF-5 Score

Change in International Index of Erectile Function-5 (IIEF-5) score. Scores range from 5 to 25, with higher scores indicating better erectile function.

Time frame
Baseline to 3 months after surgery
2

Urinary Incontinence Assessed by ICIQ-SF

Urinary continence assessed using the International Consultation on Incontinence Questionnaire-Short Form (ICIQ-SF). Scores range from 0 to 21, with higher scores indicating more severe urinary incontinence.

Time frame
1 and 3 months after surgery
3

Change in HADS Score

Change in Hospital Anxiety and Depression Scale (HADS) score. Total scores range from 0 to 42, with higher scores indicating greater anxiety and depressive symptoms.

Time frame
Baseline to 3 months after surgery
4

Change in STAI Score

Change in State-Trait Anxiety Inventory (STAI) score. Scores range from 20 to 80, with higher scores indicating greater anxiety levels.

Time frame
Baseline to 3 months after surgery

Other outcomes

Sponsors and contacts

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