Epilepsy Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
This trial has three separate groups, each with different criteria:
Group 1 – Sleep study (overnight cardiorespiratory polysomnography) group:
- People from birth up to and including 16 years of age who are scheduled for an overnight sleep and breathing study
- People who are willing and able to give their own agreement to take part, or who have a next of kin available to give consent on their behalf
- People who, in the investigator's opinion, are able to follow all study requirements
- People who can speak and read English
Group 2 – Apnoea (breathing pauses) group:
- Babies who are current inpatients in a neonatal unit, from 30 weeks gestational age up to their expected due date
- Parents who are willing and able to give consent on the baby's behalf
- Babies who, in the investigator's opinion, are able to meet all study requirements
- Families who can speak and read English
Group 3 – Epilepsy monitoring group:
- Children from birth up to under 16 years of age who are current inpatients receiving video-telemetry epilepsy monitoring
- Parents who are willing and able to give consent on the child's behalf
- Children who, in the investigator's opinion, are able and willing to follow all study requirements
- Families who can speak and read English
Who may not be able to join:
Group 1:
- Cases where the person cannot give their own consent and no next of kin is available to consent on their behalf
- Cases where the treating doctor considers the person unsuitable for the study
Group 2:
- Cases where no next of kin is available to give consent on the baby's behalf
- Cases where the treating doctor considers the baby unsuitable for the study
Group 3:
- Cases where the child cannot give their own consent and no next of kin is available to consent on their behalf
- Cases where the treating doctor considers the child unsuitable for the study
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Ross J Langley, MBChB BSc PhD MRCPCH, NHS Greater Glasgow and Clyde
Phone: 01414516582
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Assess the feasibility of collecting respiratory waveform data using Pneumowave device in patients who have (1) attended the sleep laboratory for CR- polysomnography and (2) are inpatient in neonatal unit
Can't join this trial?
Data last synced from ClinicalTrials.gov: 16 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.