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临床试验/NCT04011150
NCT04011150进行中(未招募)3 期

Development of Variable Volume Automated Mandatory Boluses (VVAMB) for Patient-controlled Epidural Analgesia During Labour and Delivery

KK Women's and Children's Hospital1 个研究点 分布在 1 个国家目标入组 197 人开始时间: 2020年8月11日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
进行中(未招募)
发起方
入组人数
197
试验地点
1
主要终点
Incidence of motor block in each group

研究概览

简要总结

A novel epidural delivery regimen was developed: Variable volume automated mandatory bolus (AMB) (VVAMB) will advance individualisation of labour epidural analgesia, by which a larger volume of bolus may contribute to better spread of the local anaesthetics within brief period and thereby reduces the chances of motor blockade that could reduce instrumental deliveries.

详细描述

Epidural analgesia is the gold standard of pain relief for labour pain. Despite this, up to 50% of parturients continue to experience pain leading to suffering and increased caregiver workload. There is also higher risk of motor blockade found in those receiving epidural analgesia, and these factors is associated with dysfunctional labour requiring obstetric intervention (instrumental delivery). Automated mandatory bolus (AMB) of variable-frequency (VAMB) has been shown to provide better pain relief as compared with conventional patient-controlled epidural analgesia (PCEA) with basal infusion, however its long lockout time per hour is associated with unsuccessful patient bolus requests, with similar motor block to conventional regimens.

The investigators therefore proposes to develop a novel epidural delivery regimen: Variable volume AMB (VVAMB) will advance individualisation of labour epidural analgesia, by which a larger volume of bolus may contribute to better spread of the local anaesthetics within brief period and thereby reduces the chances of motor blockade that could reduce instrumental deliveries. This algorithm development including pilot and clinical trial will compare VVAMB with VAMB regimens, in reducing the incidence of motor block in term women requesting for labour epidural analgesia.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Participant, Outcomes Assessor)

入排标准

年龄范围
21 Years 至 50 Years(Adult)
性别
Female
接受健康志愿者
否

入选标准

  • •Healthy (American Society of Anesthesiologists (ASA) physical status 1 and 2) primiparous parturient at term (≥36 weeks gestation);
  • •Singleton fetus;
  • •In early labor stage (cervical dilation ≤5cm);
  • •Request labor epidural analgesia and able to administer combined spinal epidural analgesia (CSEA) according to protocol.

排除标准

  • •Non-cephalic fetal presentation;
  • •Obstetric (e.g. pre-eclampsia, premature rupture of amniotic membranes for more than 48 hours, gestational diabetes on insulin, pregnancy-induced hypertension on medication) and uncontrolled medical (e.g. cardiac disease) complications;
  • •Have contraindications to neuraxial blockade or have received parenteral opioids within last 2 hours;
  • •Dural puncture/ suspected dural puncture at initiation of CSEA.

研究组 & 干预措施

Variable volume Automated Mandatory Bolus (VVAMB)

Experimental

The anaesthetic drug and pain medication are prepared in an epidural infusion pump with the VVAMB programme. The programme uses higher doses with lower frequency of medication (ropivacaine and fentanyl), and a patient control button for the patient to control the additional pain relief demands depending on the requirements during labour.

干预措施: Epidural infusion pump (Device)

Automated mandatory bolus (AMB) of variable-frequency (VAMB)

Active Comparator

The anaesthetic drug and pain medication are prepared in an epidural infusion pump with the VAMB programme. The programme uses lower doses with more frequency of medication (ropivacaine and fentanyl), and a patient control button for the patient to control the additional pain relief demands depending on the requirements during labour.

干预措施: Epidural infusion pump (Device)

Automated mandatory bolus (AMB) of variable-frequency (VAMB)

Active Comparator

The anaesthetic drug and pain medication are prepared in an epidural infusion pump with the VAMB programme. The programme uses lower doses with more frequency of medication (ropivacaine and fentanyl), and a patient control button for the patient to control the additional pain relief demands depending on the requirements during labour.

干预措施: Ropivacaine (Drug)

Variable volume Automated Mandatory Bolus (VVAMB)

Experimental

The anaesthetic drug and pain medication are prepared in an epidural infusion pump with the VVAMB programme. The programme uses higher doses with lower frequency of medication (ropivacaine and fentanyl), and a patient control button for the patient to control the additional pain relief demands depending on the requirements during labour.

干预措施: Ropivacaine (Drug)

Variable volume Automated Mandatory Bolus (VVAMB)

Experimental

The anaesthetic drug and pain medication are prepared in an epidural infusion pump with the VVAMB programme. The programme uses higher doses with lower frequency of medication (ropivacaine and fentanyl), and a patient control button for the patient to control the additional pain relief demands depending on the requirements during labour.

干预措施: Fentanyl (Drug)

Automated mandatory bolus (AMB) of variable-frequency (VAMB)

Active Comparator

The anaesthetic drug and pain medication are prepared in an epidural infusion pump with the VAMB programme. The programme uses lower doses with more frequency of medication (ropivacaine and fentanyl), and a patient control button for the patient to control the additional pain relief demands depending on the requirements during labour.

干预措施: Fentanyl (Drug)

结局指标

主要结局

Incidence of motor block in each group

时间窗: During labour (1 day)

The number of event of motor block throughout the labour. Previous studies have shown that epidural analgesia using high concentrations of local anaesthetics could lead to decreased motor functions, and are subsequently associated with an increased incidence of instrumented delivery and longer second stage of labour. In this study, the intensity of motor block is assessed by the patient's ability to move their lower extremities via a modified Bromage scale. In the modified version, a scoring of 0 implies no motor block (Free movement of both legs and feet), scoring of 1 implies partial block (Just able to flex knees with free movement of feet), 2 implies almost complete block (Unable to flex knees but with free movement of feet) and 3 implies a full block (Unable to move legs/ feet).

次要结局

  • The incidence of postnatal depression in both groups(6-10 weeks after delivery (1 day))
  • Number of subjects with Instrumental delivery(During labour (1 day))
  • Number of subjects with Breakthrough pain(During labour (1 day))
  • APGAR score(After delivery (1 day))

研究者

发起方
KK Women's and Children's Hospital
申办方类型
Other Gov
责任方
Principal Investigator
主要研究者

Sng Ban Leong

Principal Investigator

KK Women's and Children's Hospital

研究点 (1)

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