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Not yet recruitingNCT07672158TABLOUpdated Jun 26, 2026

Tranexamic Acid to Reduce Blood Loss After Varus Derotation Osteotomy

A Phase 3 interventional study of Tranexamic Acid (IV) and Placebo in Cerebral Palsy, Hip Surgery Corrective and Tranexamic Acid Use, sponsored by Murdoch Childrens Research Institute. Not yet recruiting at 1 site in Australia. Open to participants aged 4 Years to 16 Years. Per ClinicalTrials.gov, last updated 2026-06-26.

Sponsored by Murdoch Childrens Research Institute · Phase 3, Interventional, and Supportive care

Phase
Phase 3
Study type
Interventional
Enrollment
52
Allocation
Randomized
Ages
4 Years to 16 Years
Sex
All
01

Study summary

TABLO (Tranexamic Acid to reduce Blood Loss after varus derotation Osteotomy) is a clinical trial of postoperative tranexamic acid vs placebo in non-ambulatory children with cerebral palsy (CP) undergoing reconstructive hip surgery.

Improving surgical outcomes is a high priority in this patient population given the high risk of bleeding and the diminished capacity for these children to withstand substantial blood loss. Preliminary data from the study institution indicates that approximately one third of these patients receive transfusion of blood products in the postoperative period. There is growing evidence that hidden blood loss occurring in the postoperative period is substantial and can potentially be attenuated with the administration of Tranexamic Acid (TXA). However, trials on postoperative TXA have been carried out exclusively in adult surgical populations.

Read the detailed description

TABLO (Tranexamic Acid to reduce Blood Loss after varus derotation Osteotomy) is a parallel-group randomised placebo-controlled trial of postoperative tranexamic acid vs placebo in children with CP undergoing bilateral varus derotational osteotomy (VDRO) surgery. The allocation ratio is 1:1 (placebo: intervention), and the trial will be powered to detect a difference in postoperative blood loss calculated using a haemoglobin mass loss formula. Improving perioperative outcomes is a high priority in this patient population given the high risk of bleeding from this surgical intervention and the reduced physiological reserve in these children. Preliminary data from the study institution indicates that approximately one third of these patients receive transfusion of blood products in the postoperative period. There is growing evidence that hidden blood loss occurring in the postoperative period is substantial and can potentially be attenuated with the administration of Tranexamic Acid (TXA). However, trials on postoperative TXA have been carried out exclusively in adult surgical populations. This is an embedded superiority randomised placebo-controlled patient-/treating team-/assessor-blinded trial comparing tranexamic acid with placebo in reducing blood loss following bilateral bony hip reconstructive surgery in non-ambulatory children with cerebral palsy. Primary objective: to evaluate the impact of postoperative continuous intravenous TXA infusion, compared with placebo in the form of normal saline, on blood loss in non-ambulatory children with cerebral palsy undergoing bilateral VDRO surgery with or without pelvic osteotomy. Secondary objectives: to investigate the safety and tolerability of postoperative tranexamic acid in children with CP undergoing bilateral VDRO surgery with or without pelvic osteotomy, and to evaluate the health economic impact of postoperative tranexamic acid in children with cerebral palsy undergoing bilateral VDRO surgery with or without pelvic osteotomy. To the best of the study team's knowledge this will be the first randomised controlled trial to investigate postoperative intravenous TXA in a paediatric surgical population. Trial population: Non-ambulant children with cerebral palsy undergoing bilateral VDRO surgery with or without pelvic osteotomy. Planned sample size is 52 participants (26 in each group: placebo and intervention). Study setting: Single site electronic medical record (EMR) embedded trial in the software platform EpicTM at The Royal Children's Hospital (RCH). Trial intervention: after cessation of the intraoperative tranexamic acid infusion, and once the patient has been transferred to the recovery bay, the postoperative infusion will commence comprising 10mg/kg/hr intravenous TXA for 24 hours. Placebo: equivalent volume of visually identical normal saline will be infused at the same rate as the TXA. Recruitment: It is anticipated that recruitment will commence in June 2026 and cease August 2028, with the last participant completing 6-month follow up period by April 2029. Participant duration: It is anticipated that duration of participation will be approximately four to six months. The time between initial identification as potentially eligible to date of surgery is three months maximum, length of stay is approximately seven days, and post-operative follow-up is 6 months.

02

Conditions studied

  • Cerebral Palsy
  • Hip Surgery Corrective
  • Tranexamic Acid Use
  • Blood Loss, Surgical
  • Paediatrics
  • Orthopedics

Keywords

  • Cerebral Palsy
  • Hip surgery
  • Tranexamic Acid
  • Blood Loss
  • Orthopaedics
03

Who can participate

Ages eligible
4 Years to 16 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Children (aged 4 to 16 years)
  • Diagnosis of cerebral palsy (CP). CP is an umbrella term under which many specific diagnoses are captured, and the clinical team at the study institution operates a comprehensive referral network to ensure patients with any relevant diagnoses are included.
  • Gross Motor Function Classification System (GMFCS) levels IV and V, with substantial hip displacement (>40% migration percentage per Australian Hip Surveillance Guidelines (Wynter M, Gibson N, Kentish M, Love S, Thomason P, Willoughby K, et al. Australian hip surveillance guidelines for children with cerebral palsy 2014. Australian Academy of Cerebral Palsy and Developmental Medicine. 2014.)), who are on the waitlist for bilateral proximal femoral varus derotational osteotomy (VDRO) +/- unilateral or bilateral pelvic osteotomy.

Exclusion criteria

Exclusion Criteria:

  • Haematological disorder (defined as an active genetic or acquired bleeding disorder)
  • Known hypersensitivity to tranexamic acid (TXA)
  • Children with promyelocytic leukaemia being treated with oral tretinoin will be excluded from the trial because combination with TXA has resulted in fatal thrombotic complications
  • Known coagulation defect
  • Known renal disorder (moderate to severe as per study institution guidelines)
04

Study design

Phase
Phase 3
Primary purpose
Supportive care
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
52 participants (estimated)

Study arms

  • Experimental
    Tranexamic acid postoperative continuous infusion arm

    Once the patient has been transferred to recovery after surgery, the postoperative infusion will commence comprising 10mg/kg/hr intravenous tranexamic acid for 24 hours.

    Drug: Tranexamic Acid (IV)

  • Placebo comparator
    Normal saline postoperative continuous infusion arm

    The control group will receive placebo in the form of normal saline, which is physically identical to tranexamic acid and has been used in previous randomised placebo-controlled trials of tranexamic acid.

    Drug: Placebo

Interventions

  • DrugTranexamic Acid (IV)

    Once the patient has been transferred to recovery after surgery, the postoperative infusion will commence comprising 10mg/kg/hr intravenous tranexamic acid for 24 hours.

  • DrugPlacebo

    The control group will receive placebo in the form of normal saline. The volume administered will be identical to that of TXA intervention arm, and the infusion rate will be the same.

05

What researchers measure

Primary outcomes

  1. Mean change between treatment arms in postoperative haemoglobin mass loss, measured on postoperative day 5 or day of discharge (whichever is earlier) and estimated using the HAEmoglobin Mass loss DuRing the periOperative Period (HAEMDROP) formula

    HAEMDROP formula: mHb\_loss = BV\*(Hb\_initial - Hb\_final) + (TV \* 200), where: * mHb\_loss = Haemoglobin (Hb) mass loss in grams (g) * BV = Blood volume of the patient in litres (L). For paediatric patients, blood volume is \~75ml/kg. * Hb\_initial = Hb at the start of the period of interest (in grams per litre (g/L)). * Hb\_final = Hb at the end of the period of interest (in grams per litre (g/L)). * VT = volume (in L) of packed red blood cells transfused between Hb\_initial and Hb\_final. * \- 200 = 200g/L, the average haemoglobin level in a unit of blood. Multiplying this by the VT gives the haemoglobin mass transfused (in grams)

    Time frame: Day of surgery (within 15 minutes of the end of surgery), Day 5 or day of discharge (whichever is earlier)

Secondary outcomes

  1. Number of clinically significant seizures

    Seizures experienced between Day of surgery until Day 5 post-operatively which: * are more frequent or more severe than the participant's pre-admission baseline. * necessitate additional clinical monitoring or intervention, as per institutional guidelines, beyond what is expected from the participant's pre-admission baseline seizure management. * seizures which require the administration of rescue medications which deviates from what is typical for the participant at baseline.

    Time frame: Day of surgery until Day 5 post-operatively

  2. Duration of hospital stay

    Total duration of hospital stay, in calendar days, from date of admission (= day zero) to date of discharge.

    Time frame: Date of surgery, date of discharge from hospital which will be an anticipated average of 8.28 days

  3. Duration of paediatric intensive care unit admission

    The occurrence and duration of both planned and unplanned admission to the paediatric intensive care (PICU) unit during the participant's post-operative inpatient period.

    Time frame: Date of PICU admission through to date of discharge from PICU which will be an anticipated average of 26.5 hours

  4. Volume of packed red blood cells transfused

    Volume of packed red blood cells transfused during the period over which the primary outcome is measured (from end of operation to postoperative day 5 inclusive).

    Time frame: From end of operation to postoperative day 5 or day of discharge (whichever comes first)

  5. Incidence of surgical wound infections - superficial incisional surgical site infection

    Surgical site infection event defined in accordance with the Centers for Disease Control and Prevention (CDC)'s National Healthcare Safety Network (NHSN) criteria

    Time frame: Day of surgery through to 30 days following surgery

  6. Incidence of surgical wound infections - deep incisional surgical site infection

    Surgical site infection event defined in accordance with the Centers for Disease Control and Prevention (CDC)'s National Healthcare Safety Network (NHSN) criteria

    Time frame: Day of surgery through to 90 days following surgery

  7. Incidence of venous thromboembolism events requiring treatment

    Incidence of venous thromboembolism requiring anticoagulant treatment in accordance with study institution guidelines will be captured.

    Time frame: Day of surgery through to Day 5 post-surgery

  8. Changes in in quality of life, measured in quality-adjusted life years (QALYs)

    The EuroQol 5 dimensions (EQ-5D) by proxy will be completed by participants' parent/guardian. The EQ-5D is numbered from 0 to 100, where 100 means the best health you can imagine and 0 means the worst health you can imagine. From this, QALYs will be calculated and compared between intervention and control groups.

    Time frame: Preoperatively, 3 months postoperatively, 6 months postoperatively

  9. Changes in quality of life

    Changes in quality of life will be captured by the CP-CHILD (caregiver) questionnaire, which measures: Social wellbeing \& acceptance, Feelings about functioning, Participation \& physical health, Emotional wellbeing \& self-esteem, Access to services, Pain \& impact of disability, Family health

    Time frame: Preoperatively, 3 months postoperatively, 6 months postoperatively

06

Study locations

1 site
  • The Royal Children's Hospital
    Melbourne, Victoria 3052, Australia
07

References and documents

Individual participant data

Plan to share: Yes — The anonymised data set collected for the analysis of this trial will be made available 12 months following analysis and publication of the primary outcome. This includes data collected for the primary outcome and each secondary outcome.

Supporting information: Study protocol, Sap

No publications or documents are linked to this record.

08

Registry details

Key details

Study ID
NCT07672158
Lead sponsor
Murdoch Childrens Research Institute
Collaborators
University of Melbourne, Royal Children's Hospital
Responsible party
Sponsor
First posted
Jun 26, 2026
Start date
Jul 2026 (estimated)
Primary completion
Aug 2028 (estimated)
Completion
Apr 2029 (estimated)
Last update
Jun 26, 2026

Study contacts

Erich Rutz, MD, PhD
Contact
erich.rutz@rch.org.au
+61 9345 7645
Daniel Gould, MD, PhD
Contact
daniel.gould@unimelb.edu.au
+61 9345 7645
Erich Rutz, MD, PhD
principal investigator · The University of Melbourne Department of Paediatrics (Orthopaedics), The Royal Children's Hospital Melbourne

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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