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临床试验/NCT07005349
NCT07005349招募中不适用

Rule of THUMB: A Multi-centre Cluster Trial Evaluating the Implementation of a Perioperative Care Complex Intervention to Improve Outcomes From Haemorrhage During and After Caesarean Section in African Hospitals

Bruce Biccard1 个研究点 分布在 1 个国家目标入组 2,400 人开始时间: 2025年6月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
2,400
试验地点
1
主要终点
Patient assessed as high-risk for postpartum haemorrhage

研究概览

简要总结

The quality improvement project evaluating the delivery of a perioperative care complex intervention to improve haemorrhage-related outcomes in patients undergoing caesarean section. The objectives of the current study will be:

  1. To evaluate whether implementation of the 'Rule of THUMB' perioperative complex intervention increases risk assessment, diagnosis and compliance with proven interventions for haemorrhage during and after caesarean section.
  2. To understand the influence of contextual and socio-dynamic factors on how the trial results were achieved and how the intervention mechanisms did, or did not, work in practice (the process evaluation). The findings from this study will be used subsequently to modify and improve the quality improvement intervention, so that it can be delivered at scale across Africa and assess its impact on haemorrhage during and after caesarean section in the future.

详细描述

The study involves a complex intervention to improve maternal outcomes for patients undergoing caesarean section based on early diagnosis of haemorrhage during and after surgery coupled to early treatment through first-responder protocolised treatment using a care bundle of five elements called the rule of THUMB. The intervention is essentially a quality improvement programme aimed at delivering better care, care that is already known to be effective in delivering better patient outcomes. The intervention comprises two mandatory risk assessments (preoperatively in theatre and postoperatively prior to discharge from the recovery area) which are linked to hospital-specific responses. Assessments for bleeding will occur intraoperatively (through direct vision, haemodynamic changes and/or measurement of blood loss) and postoperatively (with the use of the rapid assessment tool). If bleeding is diagnosed at any point, the THUMB checklist will be used to activate bundled care. On discharge from recovery, high-risk patients will be scheduled to receive a postoperative ward visit within four hours, when a further assessment for bleeding will occur. Staff at each hospital will collect data for the two-week usual care (control) phase describing usual perioperative care. This will be followed by a period of co-design and training (2-6 weeks, as required), and then implementation of the intervention phase for a further two weeks at each hospital. The initial intervention will be modified in accordance with data collected during the usual care phase, in conjunction with local stakeholders. Further intervention refinement will occur after each period of data recruitment and analysis. Two intervention cycles will occur. The intervention is essentially a quality improvement programme aimed at delivering better care, care that is already known to be effective in delivering better patient outcomes. The intervention aims to improve compliance with recommended care for prevention and treatment of haemorrhage during and after caesarean section by creating a bundle of care that is delivered simultaneously (not sequentially) by first responders. It includes two mandated risk assessments before and after surgery, and implementation of the THUMB care bundle either in response to bleeding intraoperatively or in recovery or the ward through the rapid assessment tool.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Prevention
盲法
None

入排标准

性别
Female
接受健康志愿者

入选标准

  • Any patient who requires a caesarean section in participating countries with hospitals that routinely perform caesarean section.

排除标准

  • Patients who opt out of the trial will be excluded.

研究组 & 干预措施

Control phase

No Intervention

Control data will be collected at all hospitals over a two-week period (usual care phase). Patients in the control phase will receive the current standard postoperative care.

Intervention

Active Comparator

The intervention (a quality improvement programme) will then be implemented by the unit for all patients, aimed at delivering care that is already known to be effective in delivering better patient outcomes.

干预措施: Quality improvement program (Other)

结局指标

主要结局

Patient assessed as high-risk for postpartum haemorrhage

时间窗: 6 months

To evaluate the effect of the trial intervention on identification of high-risk patients

Administration of uterotonics intra- or postoperatively

时间窗: 6 months

To evaluate the effect of the trial intervention on administration of uterotonics

Administration of tranexamic acid intra- or postoperatively

时间窗: 6 months

To evaluate the effect of the trial intervention on administration of tranexamic acid

Uterine massage intra- or postoperatively after delivery of the baby

时间窗: 6 months

To evaluate the effect of the trial intervention on uterine massage

A postoperative clinician visit within four hours of discharge to the ward

时间窗: 6 months

To evaluate the effect of the trial intervention on clinician ward visit postoperatively

次要结局

  • Diagnosis of postpartum haemorrhage(6 months)
  • 30 day in-hospital mortality(6 months)
  • Repeat laparotomy for suspected haemorrhage(6 months)
  • Duration of hospital stay(6 months)
  • Referral to higher level of care for further management of bleeding/resuscitation(6 months)

研究者

发起方
Bruce Biccard
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Bruce Biccard

Chief Investigator

University of Cape Town

研究点 (1)

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