Context sensitive pharmacodynamics and kinetics of volatile anaesthetic agents in paediatric anaesthesia
| ISRCTN | ISRCTN31576740 |
|---|---|
| DOI | https://doi.org/10.1186/ISRCTN31576740 |
| Secondary identifying numbers | N0264132549 |
- Submission date
- 30/09/2004
- Registration date
- 30/09/2004
- Last edited
- 05/10/2009
- Recruitment status
- No longer recruiting
- Overall study status
- Completed
- Condition category
- Surgery
Prospectively registered
Protocol
Statistical analysis plan
Results
Individual participant data
Plain English summary of protocol
Not provided at time of registration
Contact information
Dr Sale
Scientific
Scientific
C/O Research & Effectiveness Department
Level 1, The Old Building
Bristol Royal Infirmary
Malborough Street
Bristol
BS2 8HW
United Kingdom
| Phone | +44 (0)117 928 3473 |
|---|---|
| r&eoffice@ubht.swest.nhs.uk |
Study information
| Study design | Randomised controlled trial |
|---|---|
| Primary study design | Interventional |
| Secondary study design | Randomised controlled trial |
| Study setting(s) | Hospital |
| Study type | Other |
| Scientific title | |
| Study objectives | To investigate the relationship between duration of anaesthesia, age of patient and quality and speed of recovery from an inhalational anaesthesia with Isoflurane or Desflurane |
| Ethics approval(s) | Not provided at time of registration |
| Health condition(s) or problem(s) studied | Surgery: Anaesthesia |
| Intervention | Prospective randomised control trial randomised to receive: 1. Isoflurane 2. Desflurane |
| Intervention type | Procedure/Surgery |
| Primary outcome measure | Not provided at time of registration |
| Secondary outcome measures | Not provided at time of registration |
| Overall study start date | 01/10/2003 |
| Completion date | 01/10/2004 |
Eligibility
| Participant type(s) | Patient |
|---|---|
| Age group | Child |
| Upper age limit | 10 Years |
| Sex | Not Specified |
| Target number of participants | 72 |
| Key inclusion criteria | 72 patients <10 years old who will require tracheal intubation and who will have minimal parenteral analgesic requirements post operatively |
| Key exclusion criteria | Does not meet inclusion criteria |
| Date of first enrolment | 01/10/2003 |
| Date of final enrolment | 01/10/2004 |
Locations
Countries of recruitment
- England
- United Kingdom
Study participating centre
C/O Research & Effectiveness Department
Bristol
BS2 8HW
United Kingdom
BS2 8HW
United Kingdom
Sponsor information
Department of Health
Government
Government
Richmond House
79 Whitehall
London
SW1A 2NL
United Kingdom
| Website | http://www.dh.gov.uk/Home/fs/en |
|---|
Funders
Funder type
Hospital/treatment centre
United Bristol Healthcare NHS Trust (UK)
No information available
Results and Publications
| Intention to publish date | |
|---|---|
| Individual participant data (IPD) Intention to share | No |
| IPD sharing plan summary | Not provided at time of registration |
| Publication and dissemination plan | Not provided at time of registration |
| IPD sharing plan |
Study outputs
| Output type | Details | Date created | Date added | Peer reviewed? | Patient-facing? |
|---|---|---|---|---|---|
| Results article | results | 01/06/2006 | Yes | No |
