Prospective randomised double blind trial of ilioinguinal nerve block versus local anaesthetic wound instillation in patients undergoing open inguinal herniorrhaphy

ISRCTN ISRCTN55731323
DOI https://doi.org/10.1186/ISRCTN55731323
Secondary identifying numbers N0170118241
Submission date
30/09/2005
Registration date
30/09/2005
Last edited
25/04/2014
Recruitment status
No longer recruiting
Overall study status
Completed
Condition category
Surgery
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 CS Ubhi
Scientific

Nottingham City Hospital
Nottingham
NG5 1PB
United Kingdom

Study information

Study designRandomised controlled trial
Primary study designInterventional
Secondary study designRandomised controlled trial
Study setting(s)Not specified
Study typeNot Specified
Scientific title
Study objectivesIs infiltration of the operative wound with local anaesthetic as effective as an inguinal nerve block?
Ethics approval(s)Not provided at time of registration
Health condition(s) or problem(s) studiedSurgery: Open inguinal herniorrhaphy
InterventionWe will audit the use of local anaesthetic in an ilioinguinal nerve block as a local anaesthetic for pain at the end of inguinal hernia, and the alternative technique of instilling local anaesthetic into the operative field at the end of surgery.
Intervention typeProcedure/Surgery
Primary outcome measureTo obtain objective information of pain relief after hernia surgery by instilling local anaesthetic and to compare the results with ilioinguinal nerve blockade.
Secondary outcome measuresNot provided at time of registration
Overall study start date11/09/2002
Completion date31/12/2003

Eligibility

Participant type(s)Patient
Age groupNot Specified
SexMale
Target number of participants60
Key inclusion criteriaA total of 60 patients, undergoing open inguinal herniorrhaphy.
Male patients listed for open repair as day case of a primary unilateral inguinal hernia under the care of two NCH consultants.
Key exclusion criteriaNo known exclusion criteria.
Date of first enrolment11/09/2002
Date of final enrolment31/12/2003

Locations

Countries of recruitment

  • England
  • United Kingdom

Study participating centre

Nottingham City Hospital
Nottingham
NG5 1PB
United Kingdom

Sponsor information

Department of Health
Government

Richmond House
79 Whitehall
London
SW1A 2NL
United Kingdom

Phone +44 (0)20 7307 2622
Email dhmail@doh.gsi.org.uk
Website http://www.dh.gov.uk/Home/fs/en

Funders

Funder type

Government

Nottingham City Hospital NHS Trust (UK), NCH Directorate R&D Budget

No information available

Results and Publications

Intention to publish date
Individual participant data (IPD) Intention to shareNo
IPD sharing plan summaryNot provided at time of registration
Publication and dissemination planNot provided at time of registration
IPD sharing plan