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Intraprostatic Injection of Tranexamic Acid Decrease Blood Loss During Monopolar TURP

Intraprostatic Injection of Tranexamic Acid Decrease Blood Loss During Monopolar TURP

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05913466
Enrollment
60
Registered
2023-06-22
Start date
2023-06-20
Completion date
2024-06-20
Last updated
2023-06-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Benign Prostatic Hyperplasia, Transurethral Resection of the Prostate, Tranexamic Acid

Brief summary

This study aims to assess the role of intraprostatic injection of tranexamic acid in decreasing the blood loss during Transurethral resection of the prostate.

Detailed description

Benign prostatic hyperplasia (BPH) is a process in which the pathology results in increased number of both stromal and epithelial cells in the area of the prostate around the urethra, which is pathologically known as hyperplasia, and not hypertrophy. The accurate cause is not well known; however, reactivation of embryonic processes is one of the hypotheses that may cause benign prostatic hyperplasia (BPH). Benign prostatic hyperplasia (BPH) is a common condition that affects elderly men. Recently, many noninvasive and mini-invasive modalities have become popular for the management of men with voiding symptoms. Transurethral resection of the prostate (TURP) is one of the most common and well-developed techniques used to treat benign prostatic hyperplasia (BPH), recognized as the 'gold standard' of the surgical treatments of enlarged prostates. The most relevant complications are the inability to void (5.8%), surgical revision (5.6%), urinary tract infection (UTI) (3.6%), bleeding requiring transfusions (2.9%), and Transurethral resection syndrome (1.4%). As the prostate has a rich blood supply, bleeding is one of the most common complications of Transurethral resection of the prostate.

Interventions

Patients in this group will receive 1 gm of Tranexamic Acid (Cyklokapron) that will be dissolved in 50 ml of injectable 0.9% saline

This group will receive 10 mL of distilled water (placebo) in 1 L of irrigation solution sterile wash (glycine).

Sponsors

Benha University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
MALE
Age
50 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

* Patient with an age between 50 and 85 years old * who had benign prostatic hyperplasia (aged 50-85 years) with a prostate weight of 50-80 g. * undergoing Transurethral resection of the prostate

Exclusion criteria

* Patient refusal. * Patients hypersensitive to Tranexamic Acid, or on antiplatelet and anticoagulant drugs. * Patients with a history of thrombotic events, bleeding disorders, chronic kidney disease. * Patients with abnormal liver function test. * Patients with cardiovascular disease and receiving with a drug-eluting stent, bladder stone, urethral stricture, or with previous prostate surgery, prostate cancer, with a UTI or who receiving 5α-reductase inhibitors.

Design outcomes

Primary

MeasureTime frameDescription
Amount of Blood Loss During Monopolar transurethral resection of the prostate2 weeks PostoperativelyThe efficacy of intraprostatic injection of tranexamic acid in reducing intraoperative bleeding will be assessed in litter.

Secondary

MeasureTime frameDescription
Hemoglobin (Hb) level2 weeks PostoperativelyThis outcome evaluates the changes in hemoglobin (Hb) level before and after the monopolar transurethral resection of the prostate (TURP) procedure.
Hematocrit (HCT) Level2 weeks PostoperativelyThis outcome evaluates the changes in hematocrit (HCT) level before and after the monopolar transurethral resection of the prostate (TURP) procedure.
Postoperative hospital stay length2 weeks PostoperativelyPostoperative hospital stay length will be assessed in days

Contacts

Primary ContactTamer Diab, MD
tamer.diab@fmed.bu.edu.eg01003583264

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 7, 2026