Ta strona została przetłumaczona automatycznie i dokładność tłumaczenia nie jest gwarantowana. Proszę odnieść się do angielska wersja za tekst źródłowy.

BLADDER STIMULATION IN PEDIATRIC EMERGENCY DEPARTMENT

12 czerwca 2026 zaktualizowane przez: Aytaç Göktuğ, Istanbul Medeniyet University

CAN THE BLADDER STIMULATION TECHNIQUE SOLVE THE URINE COLLECTION CHAOS IN THE PEDIATRIC EMERGENCY DEPARTMENT?

The purpose of this prospective, quasi-experimental study is to evaluate the efficacy of the Bladder Stimulation Technique (BST) compared to the traditional urine collection bag method in non-toilet-trained infants presenting to the Pediatric Emergency Department. The primary objective is to determine whether BST can significantly reduce urine contamination rates and the time required for successful sample collection. By comparing these two non-invasive methods, the study aims to provide a faster, cleaner, and more reliable diagnostic approach to solve the operational challenges of urine collection in acute pediatric care

Przegląd badań

Szczegółowy opis

Diagnosing urinary tract infections (UTIs) in non-toilet-trained infants is a daily and critical challenge in pediatric emergency departments. In this highly vulnerable group, a UTI can rapidly progress to severe complications, making an accurate diagnosis via a sterile or very clean urine sample absolutely essential. Currently, the most common non-invasive method for collecting urine from these infants is the adhesive urine bag. However, this method has significant drawbacks. Bag samples have notoriously high contamination rates-often exceeding 50%-because bacteria from the baby's skin or stool easily mix with the urine.

When a urine sample is contaminated, it frequently leads to false-positive results. This forces physicians to either prescribe unnecessary antibiotics to a very young infant or subject the baby to invasive, painful procedures like urethral catheterization to secure a sterile sample. Furthermore, waiting for an infant to naturally void into a bag is highly unpredictable, often taking hours. This waiting period increases the length of hospital stays, frustrates parents, and creates operational bottlenecks in busy emergency departments.

The Proposed Intervention: Bladder Stimulation Technique (BST) To address these clinical and operational challenges, clinicians are exploring alternative non-invasive methods. The Bladder Stimulation Technique (BST) is a safe, completely non-invasive maneuver that involves gently tapping and massaging the infant's lower abdomen (suprapubic area) and lower back (lumbar region) in a specific sequence. This gentle stimulation triggers the infant's natural reflex to urinate, allowing healthcare providers to catch a midstream urine sample directly into a sterile container.

Study Design and Methodology This is a prospective, quasi-experimental comparative study conducted in a high-volume Pediatric Emergency Department. The study is designed to directly compare the traditional adhesive urine bag method with the Bladder Stimulation Technique.

The study will specifically include infants younger than 6 months of age who present to the emergency department and require a urine sample for clinical evaluation. Eligible infants will be evaluated using one of the two collection methods, and the study will rigorously track and compare the outcomes of both approaches in real-time.

Primary and Secondary Objectives

The study focuses on three main questions regarding this specific age group:

Contamination Rates: Does BST provide a cleaner urine sample compared to the bag method in infants under 6 months, thereby significantly reducing the rate of false-positive cultures?

Time Efficiency: Does BST reduce the time required to successfully collect a urine sample compared to waiting for a bag collection?

Success Rate: What is the overall success rate of obtaining a viable urine sample using BST versus the bag method within a standard emergency room timeframe? The findings of this study have the potential to immediately change clinical guidelines and daily practices in acute pediatric care. If the Bladder Stimulation Technique proves to be faster and less prone to contamination than the traditional bag method, it will serve as a crucial "diagnostic firewall." For parents, this means less time waiting in the emergency room, protection from unnecessary antibiotic treatments, and avoiding the pain and trauma of invasive catheterization for their babies. For healthcare systems, it offers a cost-effective, evidence-based solution to resolve diagnostic dilemmas and operational bottlenecks in emergency departments.

Typ studiów

Interwencyjne

Zapisy (Szacowany)

124

Faza

  • Nie dotyczy

Kontakty i lokalizacje

Ta sekcja zawiera dane kontaktowe osób prowadzących badanie oraz informacje o tym, gdzie badanie jest przeprowadzane.

Lokalizacje studiów

Kryteria uczestnictwa

Badacze szukają osób, które pasują do określonego opisu, zwanego kryteriami kwalifikacyjnymi. Niektóre przykłady tych kryteriów to ogólny stan zdrowia danej osoby lub wcześniejsze leczenie.

Kryteria kwalifikacji

Wiek uprawniający do nauki

  • Dziecko

Akceptuje zdrowych ochotników

Nie

Opis

Inclusion Criteria:

  • Infants strictly under 6 months of age.
  • Patients presenting to the pediatric emergency department who require a urine sample collection for any clinical indication (e.g., fever without a source, suspected urinary tract infection).
  • Infants who are able to be fed orally or enterally (as the protocol requires the procedure to be performed 20 minutes after feeding to ensure bladder volume).
  • Presence of informed written consent from a parent or legal guardian.

Exclusion Criteria:

  • Infants aged 6 months or older.
  • Patients requiring immediate life-saving resuscitation or those who are hemodynamically unstable.
  • Patients with known congenital anomalies of the genitourinary tract.
  • Patients with known neurological disorders that may affect normal bladder function or voiding reflexes (e.g., neural tube defects, spina bifida).
  • Presence of skin lesions, active infections, trauma, or surgical incisions in the paravertebral (lower back) or suprapubic (lower abdomen) areas that would contraindicate physical massage and tapping.
  • Patients with any clinical contraindication to feeding.
  • Refusal of parental consent.

Plan studiów

Ta sekcja zawiera szczegółowe informacje na temat planu badania, w tym sposób zaprojektowania badania i jego pomiary.

Jak projektuje się badanie?

Szczegóły projektu

  • Główny cel: Diagnostyczny
  • Przydział: Nielosowe
  • Model interwencyjny: Przydział równoległy
  • Maskowanie: Brak (otwarta etykieta)

Broń i interwencje

Grupa uczestników / Arm
Interwencja / Leczenie
Eksperymentalny: Arm 1: Bladder Stimulation Technique
Infants in this arm will undergo the Bladder Stimulation Technique. This completely non-invasive method involves a specific sequence of paravertebral (lower back) massage and suprapubic (lower abdomen) tapping to trigger the infant's natural voiding reflex, allowing for a midstream urine sample to be collected directly into a sterile container.
In the intervention group, the Bladder Stimulation Technique (BST) was performed. The infant was held safely suspended in the air by their armpits by a researcher to relax the abdominal muscles. The physician then initiated a stimulation cycle consisting of 30 seconds of gentle paravertebral (lower back) massage, followed immediately by 30 seconds of light suprapubic (lower abdomen) tapping. This 1-minute cycle was repeated continuously for a maximum of 5 minutes. The moment the natural voiding reflex was triggered and the infant began to urinate, a midstream urine sample was directly caught into a sterile specimen container
Aktywny komparator: Arm 2: Traditional Urine Bag Method
Infants in this arm will undergo the current standard of care. A standard, sterile adhesive urine collection bag will be applied to the infant's perineal area. The patient will be monitored until natural voiding occurs into the bag
The current standard care method for urine collection in non-toilet-trained infants. The infant's perineal area is cleaned, and a standard, sterile pediatric adhesive urine collection bag is attached. The infant is then closely monitored in the emergency department until spontaneous natural voiding occurs into the bag.

Co mierzy badanie?

Podstawowe miary wyniku

Miara wyniku
Opis środka
Ramy czasowe
Success Rate of the Bladder Stimulation Technique and Influencing Factors
Ramy czasowe: From the start of the stimulation maneuver until at least 1 cc of urine is obtained (maximum of 5 minutes)
The primary objective is to evaluate the percentage of successful urine collections, strictly defined as obtaining at least 1 cc (mL) of clean-catch midstream urine, achieved specifically by using bladder stimulation maneuvers (paravertebral massage and suprapubic tapping). Additionally, this outcome evaluates the clinical and demographic factors (e.g., patient age, gender, weight) that influence the success of this specific maneuver.
From the start of the stimulation maneuver until at least 1 cc of urine is obtained (maximum of 5 minutes)

Miary wyników drugorzędnych

Miara wyniku
Opis środka
Ramy czasowe
Effect on Emergency Department Waiting Time
Ramy czasowe: Up to 5 minutes for the bladder stimulation group, and until at least 1 cc of urine is obtained for the traditional bag group
To evaluate and compare the effect of both urine collection methods (the bladder stimulation technique versus the traditional adhesive bag) on the total waiting time in the emergency department, measured from the initiation of the procedure until at least 1 cc of urine is successfully obtained.
Up to 5 minutes for the bladder stimulation group, and until at least 1 cc of urine is obtained for the traditional bag group

Inne miary wyników

Miara wyniku
Opis środka
Ramy czasowe
Effect on Specimen Contamination Rates
Ramy czasowe: Up to 72 hours
To evaluate and compare the effect of both urine collection methods on the rates of urine culture contamination, in order to determine which method yields more reliable clinical samples.
Up to 72 hours

Współpracownicy i badacze

Tutaj znajdziesz osoby i organizacje zaangażowane w to badanie.

Daty zapisu na studia

Daty te śledzą postęp w przesyłaniu rekordów badań i podsumowań wyników do ClinicalTrials.gov. Zapisy badań i zgłoszone wyniki są przeglądane przez National Library of Medicine (NLM), aby upewnić się, że spełniają określone standardy kontroli jakości, zanim zostaną opublikowane na publicznej stronie internetowej.

Główne daty studiów

Rozpoczęcie studiów (Rzeczywisty)

1 lutego 2026

Zakończenie podstawowe (Rzeczywisty)

30 kwietnia 2026

Ukończenie studiów (Szacowany)

15 czerwca 2026

Daty rejestracji na studia

Pierwszy przesłany

12 czerwca 2026

Pierwszy przesłany, który spełnia kryteria kontroli jakości

12 czerwca 2026

Pierwszy wysłany (Rzeczywisty)

17 czerwca 2026

Aktualizacje rekordów badań

Ostatnia wysłana aktualizacja (Rzeczywisty)

17 czerwca 2026

Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości

12 czerwca 2026

Ostatnia weryfikacja

1 czerwca 2026

Więcej informacji

Terminy związane z tym badaniem

Inne numery identyfikacyjne badania

  • IstabulMU-PED-AG-01

Plan dla danych uczestnika indywidualnego (IPD)

Planujesz udostępniać dane poszczególnych uczestników (IPD)?

NIE

Informacje o lekach i urządzeniach, dokumenty badawcze

Bada produkt leczniczy regulowany przez amerykańską FDA

Nie

Bada produkt urządzenia regulowany przez amerykańską FDA

Nie

Te informacje zostały pobrane bezpośrednio ze strony internetowej clinicaltrials.gov bez żadnych zmian. Jeśli chcesz zmienić, usunąć lub zaktualizować dane swojego badania, skontaktuj się z register@clinicaltrials.gov. Gdy tylko zmiana zostanie wprowadzona na stronie clinicaltrials.gov, zostanie ona automatycznie zaktualizowana również na naszej stronie internetowej .

Badania kliniczne na Bladder Stimulation Technique

Subskrybuj