A randomised controlled trial investigating the efficacy of a local anaesthetic infusion pump for postoperative analgesia in arthroscopic subarachnoid decompression
| ISRCTN | ISRCTN38563644 |
|---|---|
| DOI | https://doi.org/10.1186/ISRCTN38563644 |
| Protocol serial number | N0188097521 |
| Sponsor | Department of Health |
| Funder | Lancashire Teaching Hospitals NHS Trust (UK) |
- Submission date
- 30/09/2004
- Registration date
- 30/09/2004
- Last edited
- 08/04/2014
- Recruitment status
- No longer recruiting
- Overall study status
- Completed
- Condition category
- Signs and Symptoms
Prospectively registered
Protocol
Statistical analysis plan
Results
Individual participant data
Record updated in last year
Plain English summary of protocol
Not provided at time of registration
Contact information
Mr S Bale
Scientific
Scientific
Orthopaedics
Lancashire Teaching Hospitals NHS Trust
Preston
PR2 9HT
United Kingdom
Study information
| Primary study design | Interventional |
|---|---|
| Study design | Randomised controlled trial |
| Secondary study design | Randomised controlled trial |
| Scientific title | |
| Study objectives | Does the pump reduce oral analgesic requirements and reduce pain scores? |
| Ethics approval(s) | Not provided at time of registration |
| Health condition(s) or problem(s) studied | Signs and Symptoms: Pain |
| Intervention | 1. One group will receive local anaesthetic in and around the operated area plus pain management. 2. The other group will have the anaesthetic infusion pump attached. |
| Intervention type | Other |
| Primary outcome measure(s) |
Visual analogue pain scores and oral analgesia intake will be measured every day for seven days following surgery |
| Key secondary outcome measure(s) |
Not provided at time of registration |
| Completion date | 01/12/2006 |
Eligibility
| Participant type(s) | Patient |
|---|---|
| Age group | Not Specified |
| Sex | Not Specified |
| Target sample size at registration | 25 |
| Key inclusion criteria | Not provided at time of registration |
| Key exclusion criteria | Not provided at time of registration |
| Date of first enrolment | 01/08/2001 |
| Date of final enrolment | 01/12/2006 |
Locations
Countries of recruitment
- United Kingdom
- England
Study participating centre
Orthopaedics
Preston
PR2 9HT
United Kingdom
PR2 9HT
United Kingdom
Results and Publications
| Individual participant data (IPD) Intention to share | No |
|---|---|
| IPD sharing plan summary | Not provided at time of registration |
| IPD sharing plan |