Randomised controlled trial comparing the efficacy of ambulatory local anaesthetic infusion pump versus femoral nerve block in day case anterior cruciate ligament (ACL) reconstruction
| ISRCTN | ISRCTN87195445 |
|---|---|
| DOI | https://doi.org/10.1186/ISRCTN87195445 |
| Protocol serial number | N0188139053 |
| Sponsor | Department of Health |
| Funder | Lancashire Teaching Hospitals NHS Trust (UK) |
- Submission date
- 30/09/2004
- Registration date
- 30/09/2004
- Last edited
- 24/08/2015
- 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 J Shaw
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 | Randomised controlled trial comparing the efficacy of ambulatory local anaesthetic infusion pump versus femoral nerve block in day case anterior cruciate ligament (ACL) reconstruction |
| Study objectives | To determine the most effective form of postoperative analgesia in day case ACL surgery. This could enhance patient acceptance and satisfaction of day case ACL reconstruction in the future. |
| Ethics approval(s) | Not provided at time of registration |
| Health condition(s) or problem(s) studied | Signs and Symptoms: Post-operative pain |
| Intervention | Comparison of local anaesthetic infusion pump with the femoral nerve block for post operative analgesia in day case ACL surgery |
| Intervention type | Procedure/Surgery |
| Primary outcome measure(s) |
Not provided at time of registration |
| 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 | 50 |
| Key inclusion criteria | Not provided at time of registration |
| Key exclusion criteria | Not provided at time of registration |
| Date of first enrolment | 01/01/2004 |
| Date of final enrolment | 01/12/2006 |
Locations
Countries of recruitment
- United Kingdom
- England
Study participating centre
Lancashire Teaching Hospitals NHS Trust
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 |
