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Assessment of the sympathetic nervous system blockade of the upper limb after a brachial plexus block in patients receiving haemodialysis

Assessment of the sympathetic nervous system blockade of the upper limb after a brachial plexus block in patients receiving haemodialysis: an observational single centre cohort study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ISRCTN
Registry ID
ISRCTN82322174
Enrollment
30
Registered
2010-02-12
Start date
2010-02-10
Completion date
Unknown
Last updated
2015-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Renal failure Urological and Genital Diseases Unspecified renal failure

Interventions

Subjects will have a measure of their forearm blood flow made on three occasions: 1. Immediately before the insertion of the regional block for surgery 2. Immediately after the insertion of the regio

Sponsors

Nottingham University Hospitals NHS Trust (UK)
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1. Patients with end stage renal failure 2. Over 18 years of age, either sex 3. Written consent obtained 4. Due to undergo surgery for forearm fistula creation under a regional block

Exclusion criteria

Exclusion criteria: 1. Smokers 2. Damaged skin on the arm 3. Circulatory disorders such as Raynaud's disease, systemic sclerosis, sickle cell trait or disease 4. Current use of beta blockers 5. Undergoing haemodialysis for more than 12 months

Design outcomes

Primary

MeasureTime frame
1. The transient hyperaemic response ratio (THRR) will be calculated for each compression using the formula THRR = F2/F1 where F1 is the initial fall in blood flow flux following compression of the brachial artery and F2 is the hyperaemic response following its release. The mean of each set of readings will be taken and compared with the subjects' normal values using a paired t-test. 2. Skin temperature will be compared before and after the regional block and dialysis using a t-test Measured at pre-regional block, immediately post-regional block onset, and 4 hours after regional block.

Secondary

MeasureTime frame
No secondary outcome measures

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026