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Prophylactic Anticoagulation for Central Venous Line Insertion in Critically Ill Children

13. juli 2026 oppdatert av: Hani Hamed Saad, Menoufia University

Prophylactic Anticoagulation Versus Standard Care at Central Venous Line Insertion in Critically Ill Children: A Randomized Controlled Study

This will be a Prospective, randomized, open- label, parallel-group, center trial, which will include 80 of Children which will be admitted at Pediatric Intensive Care Unit (PICU) of Menoufia university Hospital from August 2026 to Mars 2027.

Aim of the study will be:

  1. Compare the incidence of clinically significant catheter-related complications (catheter occlusion requiring intervention or catheter-related thrombosis) within 14 days after CVL insertion between children receiving prophylactic anticoagulation and those receiving standard care.
  2. Compare time-to- first catheter occlusion.
  3. Compare rate of catheter-related bloodstream infection (CLABSI) within 30 days.
  4. Compare number of catheter manipulations and unplanned catheter removals.
  5. Compare major and minor bleeding events.
  6. Assess catheter dwell time and need for thrombolysis or therapeutic anticoagulation.

Studieoversikt

Detaljert beskrivelse

The study population will be divided into two groups:

  1. Enoxaparin Group (Anticoagulation Arm):

    This group will receive prophylactic anticoagulation with enoxaparin in accordance with institutional guidelines for prophylactic anticoagulation in Pediatric patients.

  2. Usual Care Group (Control Arm):

This group will receive standard care without prophylactic anticoagulation.

All patients in this study will be subjected to:

A- Demographic and clinical data Collection:

  • Patient demographics: age, sex, body mass index (BMI) and the primary diagnosis.
  • CVC characteristics: type of line, number of lumens, catheter size, site and laterality, and date of insertion and removal.
  • Thrombotic events: date of thrombus detection, affected blood vessel (confirmed by Doppler ultrasound), and anticoagulation details (type, dose, and duration. (
  • Anticoagulant use: agent used (e.g., LMWH), initiation timing and monitoring. B- Full clinical examination will be done including vital signs (HR, RR, BP, temperature) for each child.

C- Investigations will be done including the following:

Laboratory Analysis: CBC, Platelet counts at baseline, day 3-5, for monitoring heparin- related thrombocytopenia, CRP, Electrolytes, Blood culture, Urea, creatinine, ALT, AST and D-dimer level.

Radiological: Ultrasound of catheterized vessel if clinical suspicion of thrombosis; consider scheduled ultrasound on day 7 and 14.

Intervention and Monitoring

Enoxaparin Group (Intervention Arm):

  • Children randomized to receive enoxaparin will be administered enoxaparin subcutaneously every 12 hours, with dosing based on age and weight as follows:

    1. 0.75mg/kg for children ≤2 months old.
    2. 0.5 mg/kg (maximum 30 mg) for children >2 months old.
  • Doses will be adjusted for obesity and renal insufficiency as needed.
  • The first dose will be given within 24 hours of CVC insertion. The dose will be adjusted to achieve a target anti-Xa level of 0.2-0.5 IU/mL.
  • Anti-Xa levels will be measured locally 4-6 hours after every third dose, and dosing will be adjusted accordingly until the target range is reached. Once therapeutic range is achieved, anti-Xa monitoring will be performed weekly.
  • Enoxaparin will be discontinued in the event of a clinically significant bleeding episode. It will be resumed 24 hours after correction of any coagulopathy, as confirmed by clinical and laboratory parameters.

Usual Care Group (Control Arm):

Children randomized to usual care will not receive anticoagulation. Standard CVC care procedures will be followed according to PICU protocols.

Monitoring for Thrombosis and Bleeding

  1. All children will undergo daily clinical monitoring for signs of bleeding.
  2. To evaluate catheter-related thrombosis, ultrasound imaging of the vein proximal and distal to the CVC insertion site.
  3. To assess coagulation profile and thrombotic risk, blood samples will be drawn at the following time points:

    1. On the day of CVC insertion
    2. The day after insertion
    3. Day 4 after insertion

Studietype

Intervensjonell

Registrering (Antatt)

40

Fase

  • Ikke aktuelt

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiekontakt

Studer Kontakt Backup

  • Navn: Nagwan Yossery Saleh, MD, Pediatrics
  • Telefonnummer: +201003961071
  • E-post: drnagwan80@gmail.com

Studiesteder

    • Menoufia Governorate
      • Shibīn al Kawm, Menoufia Governorate, Egypt
        • Menoufia university hospital, Pediatric intensive care unit
        • Ta kontakt med:
        • Ta kontakt med:
        • Underetterforsker:
          • Nagwan Yossery Saleh, MD, pediatrics
        • Underetterforsker:
          • Amira Zaki Badawy, MD, clinical pathology

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

  • Barn
  • Voksen

Tar imot friske frivillige

Nei

Beskrivelse

Inclusion Criteria:

1)- All Children requiring a newly placed central venous line (peripherally inserted central catheter [PICC], or non-tunneled central venous catheter) for clinical care.

Exclusion Criteria:

  1. - Known major congenital bleeding diathesis or platelet count <50,000/µL at time of insertion.
  2. - Already on therapeutic anticoagulation for another indication.
  3. - Known heparin allergy or history of heparin-induced thrombocytopenia.
  4. - Use of dialysis catheters (study focuses on standard CVCs/PICCs).

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Forebygging
  • Tildeling: N/A
  • Intervensjonsmodell: Enkeltgruppeoppdrag
  • Masking: Ingen (Open Label)

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Aktiv komparator: 1- Enoxaparin Group (Anticoagulation Arm)
This group will receive prophylactic anticoagulation with enoxaparin in accordance with institutional guidelines for prophylactic anticoagulation in Pediatric patients.

Enoxaparin Group (Intervention Arm):

This group will receive prophylactic anticoagulation with enoxaparin in accordance with institutional guidelines for prophylactic anticoagulation in Pediatric patients.

  • Children randomized to receive enoxaparin will be administered enoxaparin subcutaneously every 12 hours, with dosing based on age and weight as follows:

    1. 0.75mg/kg for children ≤2 months old.
    2. 0.5 mg/kg (maximum 30 mg) for children >2 months old. Doses will be adjusted for obesity and renal insufficiency as needed.
  • The first dose will be given within 24 hours of CVC insertion. The dose will be adjusted to achieve a target anti-Xa level of 0.2-0.5 IU/mL.
  • Anti-Xa levels will be measured locally 4-6 hours after every third dose, and dosing will be adjusted accordingly until the target range is reached. Once therapeutic range is achieved, anti-Xa monitoring will be performed weekly.
  • Enoxaparin will be discontinued in the event of a clinically significant bleeding episode. I

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Incidence of catheter-related venous thrombosis
Tidsramme: 14 days
Incidence (%) of catheter-related venous thrombosis within 14 days following central venous catheter placement, diagnosed using duplex ultrasonography. Both symptomatic thrombosis (clinically suspected and confirmed by imaging) and asymptomatic thrombosis (identified by protocol-specified ultrasound screening at Day 7-14) will be included. Outcome adjudication will be performed by an independent blinded committee.
14 days

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Incidence of catheter patency
Tidsramme: Day 7 and Day 14
Percentage of participants with a functioning central venous catheter without need for replacement or fibrinolytic therapy at Day 7 and Day 14.
Day 7 and Day 14
Percentage of participants who develop catheter-related bloodstream infection, diagnosed according to CDC criteria.
Tidsramme: 30 days
Percentage of participants who develop catheter-related bloodstream infection
30 days
Incidence of major bleeding
Tidsramme: 14 days
Percentage of participants experiencing major bleeding within 14 days, defined as bleeding causing hemodynamic instability, requiring blood transfusion, surgical intervention, or resulting in intracranial hemorrhage.
14 days
Incidence of minor bleeding
Tidsramme: 14 days
Percentage of participants experiencing minor bleeding not fulfilling criteria for major bleeding.
14 days
Catheter removal due to thrombosis
Tidsramme: 30 days
Percentage of participants requiring catheter removal because of confirmed catheter-related thrombosis.
30 days
Catheter dwell time
Tidsramme: 30 days
Duration of central venous catheter placement measured in days from insertion until catheter removal.
30 days
All-cause in-hospital mortality
Tidsramme: During hospitalization (up to 30 days)
Percentage of participants who die from any cause during hospitalization.
During hospitalization (up to 30 days)

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Etterforskere

  • Hovedetterforsker: Hani Hamed Saad, MD, pediatrics, Faculty of medicine, Menoufia University

Publikasjoner og nyttige lenker

Den som er ansvarlig for å legge inn informasjon om studien leverer frivillig disse publikasjonene. Disse kan handle om alt relatert til studiet.

Hjelpsomme linker

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Antatt)

1. august 2026

Primær fullføring (Antatt)

31. juli 2027

Studiet fullført (Antatt)

31. august 2027

Datoer for studieregistrering

Først innsendt

2. juli 2026

Først innsendt som oppfylte QC-kriteriene

13. juli 2026

Først lagt ut (Faktiske)

17. juli 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

17. juli 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

13. juli 2026

Sist bekreftet

1. juli 2026

Mer informasjon

Begreper knyttet til denne studien

Plan for individuelle deltakerdata (IPD)

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NEI

Legemiddel- og utstyrsinformasjon, studiedokumenter

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Nei

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Nei

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