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Labour clinical trials

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NCT ID: NCT03515616 Recruiting - Labour Clinical Trials

Evaluation of Labour Progress by PC Angle

Start date: May 7, 2018
Phase:
Study type: Observational

- Ultrasound during first stage of labour has a very important role in prediction of mode of delivery

NCT ID: NCT02838329 Recruiting - Ropivacaine Clinical Trials

Labour Epidural Top-up With Warmed Ropivacaine

LETWR
Start date: July 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to determine weather using warmed (body temperature) 0.75% Ropivicaine to convert labour epidural analgesia to surgical anaesthesia, reduces the onset time of surgical block, compared to standard room temperature

NCT ID: NCT02116842 Recruiting - Pregnancy Clinical Trials

Minimum Effective Dose (MED) & Epidural Bupivacaine

Start date: December 2012
Phase: Phase 4
Study type: Interventional

Local anaesthetics are highly toxic drugs. They can cause toxicity by an absolute overdose, accidental injection in a blood vessel or slow absorption from the area of injection. The risk of toxicity when performing regional anaesthesia can be reduced significantly by injecting the optimal dose of local anaesthetic at the correct site. To date most of the local anaesthetic dose finding studies for epidural labour analgesia has focused on ED50 ( the dose effective in 50% of patients). The purpose of this research study is to find out the ED95 dose (the dose effective in 95% of patients) of local anaesthetic for epidural analgesia in labour. The dose determined from this research trial will guide the anaesthetists to the optimal starting dose of the local anaesthetics for epidural analgesia in labour. This would lead to decreased chances of toxicity and will improve patient safety. We aim to recruit a total of 100 pregnant patients in early labour (cervical dilatation ≤ 5 cm) requesting epidural analgesia to answer the research question based on the continual reassessment method. Patients will be recruited according to well-defined criteria. They will be fully informed about the study and have the choice of not participating or opting out at any time during the study. It is not going to affect the kind of treatment they receive. The experts in the field with full safety precautions will perform this study at St James' Hospitals, Leeds.