Randomised double-blind prospective controlled trial of intercostal nerve block for post-operative pain after bilateral thoracoscopic sympathectomy

ISRCTN ISRCTN05813093
DOI https://doi.org/10.1186/ISRCTN05813093
Protocol serial number N0123138366
Sponsor Department of Health
Funder University Hospitals of Leicester NHS Trust (UK)
Submission date
30/09/2004
Registration date
30/09/2004
Last edited
21/03/2017
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

Dr David Raitt
Scientific

University Hospitals of Leicester
c/o Research and Development Office
Leicester General Hospital NHS Trust
Leicester
LE1 4PW
United Kingdom

Phone +44 (0)116 258 4109
Email nicola.turner@uhl-tr.nhs.uk

Study information

Primary study designInterventional
Study designRandomised double-blind prospective controlled trial
Secondary study designRandomised controlled trial
Study type Participant information sheet
Scientific titleRandomised double-blind prospective controlled trial of intercostal nerve block for post-operative pain after bilateral thoracoscopic sympathectomy
Study objectivesTo assess the efficacy of thoracoscopic intercostal nerve block by laevobupivacaine in alleviating immediate postoperative pain in patients undergoing bilateral thoracoscopic sympathectomy
Ethics approval(s)Not provided at time of registration
Health condition(s) or problem(s) studiedPost-operative pain
InterventionRandomised double-blind prospective controlled trial
Intervention typeDrug
PhaseNot Applicable
Drug / device / biological / vaccine name(s)Laevobupivacaine
Primary outcome measure(s)

An assessment of the efficacy of thoracoscopic intercostal nerve block by laevobupivacaine in alleviating immediate postoperative pain in patients undergoing bilateral thoracoscopic sympathectomy

Key secondary outcome measure(s)

Not provided at time of registration

Completion date31/07/2003

Eligibility

Participant type(s)Patient
Age groupAdult
SexAll
Key inclusion criteriaPatients having undergone bilateral thoracoscopic sympathectomy
Key exclusion criteriaNot provided at time of registration
Date of first enrolment01/08/2002
Date of final enrolment31/07/2003

Locations

Countries of recruitment

  • United Kingdom
  • England

Study participating centre

University Hospitals of Leicester
Leicester
LE1 4PW
United Kingdom

Results and Publications

Individual participant data (IPD) Intention to shareNo
IPD sharing plan summaryNot provided at time of registration
IPD sharing plan

Study outputs

Output type Details Date created Date added Peer reviewed? Patient-facing?
Participant information sheet Participant information sheet 11/11/2025 11/11/2025 No Yes

Editorial Notes

21/03/2017: No publications found, verifying study status with principal investigator.