Breakthrough Pain

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Review clinical trials related to Breakthrough Pain. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Programmed Intermittent Epidural Bolus Compared With Continuous Infusion in Multiparous Women

The goal of this randomized controlled trial is to examine the impact of programmed intermittent bolus epidural analgesia technique on the incidence of breakthrough pain during labor in multiparous women compared to continuous epidural infusion. multiparous women will randomly be divided during labor into two groups; study group will receive mix of Bupivacaine and fentanyl once (bolus) every 60 minutes; the control group will receive continuously the same dose during an hour, until delivery.

Participants needed: 186
Trial details
Biological sex: FemaleType: InterventionalSponsor: Holy Family Hospital, Nazareth, IsraelUpdated: Apr 13, 2026Locations: 1
Eligibility criteria

multiparous women [+6]

Estimated fetal weight greater than 4.0 kg [+2]

Status: Recruiting

PIEB Compared With CEI on Breakthrough Pain in Nulliparous Women

The goal of this randomized controlled trial is to examine the impact of programmed intermittent bolus epidural analgesia technique on the incidence of breakthrough pain during labor in nulliparous women compared to continuous epidural infusion. Nulliparous women will randomly be divided during labor into two groups; study group will receive mix of Bupivacaine and fentanyl once (bolus) every 60 minutes; the control group will receive continuously the same dose during an hour, until delivery.

Participants needed: 240
Trial details
Biological sex: FemaleType: InterventionalSponsor: Holy Family Hospital, Nazareth, IsraelUpdated: Apr 13, 2026Locations: 1
Eligibility criteria

Nulliparous women [+6]

Estimated fetal weight > 4 kg [+4]

Status: Not yet recruiting

Paediatric Breakthrough Pain Assessment

Many children and young people with life-limiting and life-threatening illnesses get sudden bursts of pain called breakthrough pain. At the moment, there aren't any good ways to measure this pain in children and young people. The investigators are developing two questionnaires to help: one for patients to fill out themselves and another for parents or healthcare professionals to complete for younger children and young people who cannot explain their pain for themselves. The investigators plan to work with 210 people across hospitals and hospices in England and Wales. This includes children and young people with life-limiting and life-threatening illnesses, their caregivers, and healthcare professionals. The investigators have already made a first version of the questionnaires. The project has three main Studies: In Study 1, the investigators will talk to 5-10 young patients and 5-10 caregivers about their experiences with breakthrough pain. The investigators will use their feedback to improve the questionnaires. In Study 2, the investigators will ask 5-10 patients, 5-10 caregivers, and 5-10 healthcare professionals to fill out the questionnaires while speaking their thoughts out loud. This will help the investigators find any parts that are confusing or difficult to understand. In Study 3, the investigators will test how well the questionnaires works. 80 patients, 40 caregivers, and 40 healthcare professionals will complete the questionnaires three different times to make sure they measure breakthrough pain as accurately as possible. These questionnaire will be useful for hospitals and hospices across England and Wales to help them better manage pain, including breakthrough pain, in patients aged 3 months to 25 years who have life-limiting and life-threatening illnesses.

Participants needed: 210
Trial details
Age: 8-99Biological sex: AllType: ObservationalSponsor: University of SouthamptonUpdated: Jan 24, 2025
Eligibility criteria

Children and young people aged 8-25 years who have experienced 1) background pai... [+6]

• Children, young people, parents and caregivers with limited ability to communi... [+2]

Status: Recruiting

Development of Variable Volume Automated Mandatory Boluses for Patient-controlled Epidural Analgesia During Labour

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.

Participants needed: 216
Trial details
Phase: Phase 3Age: 21-50Biological sex: FemaleType: InterventionalSponsor: KK Women's and Children's HospitalUpdated: Oct 9, 2024Locations: 1
Eligibility criteria

Healthy (American Society of Anesthesiologists (ASA) physical status 1 and 2) pr... [+3]

Non-cephalic fetal presentation; [+3]