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Analgesic efficacy of repetitive nerve blockade after major ankle and hindfoot surgery - A feasibility study

Analgesic efficacy of repetitive nerve blockade after major ankle and hindfoot surgery - A feasibility study

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
EU CTR
Registry ID
EUCTR2020-000294-24-DK
Enrollment
16
Registered
2020-06-24
Start date
2020-08-18
Completion date
Unknown
Last updated
2022-04-19

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

Conditions

Major ankle and hindfoot surgery MedDRA version: 20.0 Level: LLT Classification code 10038286 Term: Regional nerve block System Organ Class: 100000004865

Interventions

Trade Name: Marcain Adrenalin Product Name: Marcain Adrenalin Product Code: N 01 BB 01 Pharmaceutical Form: Concentrate and solvent for solution for injection/infusion INN or Proposed INN: Bupivacaine

Sponsors

Aarhus University Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Major ankle and hindfoot surgery Age older than 18 years ASA 1-3 Informed consent Are the trial subjects under 18? no Number of subjects for this age range: F.1.2 Adults (18-64 years) yes F.1.2.1 Number of subjects for this age range 8 F.1.3 Elderly (>=65 years) yes F.1.3.1 Number of subjects for this age range 8

Exclusion criteria

Exclusion criteria: Patients who cannot cooperate with the investiagation Patients who do not speak and understand danish Allergy to drugs used in the study Diabetis mellitus Chronic pain (and daily opioid usage) Pregnancy Fertile women, who do not use contraception

Design outcomes

Primary

MeasureTime frame
Main Objective: The purpose of the study is to demonstrate that repetitive nerveblockade with a protracted mixture of local anesthetic can provide postoperative analgesia for 48 h after major ankle and hindfoot surgery.;Secondary Objective: Non applicable;Primary end point(s): Cumulated opioid usage 48 h postoperatively;Timepoint(s) of evaluation of this end point: 48 h postoperative

Secondary

MeasureTime frame
Secondary end point(s): Time to first opioid usage because of pain (NRS > 3) NRS score 0, 6, 12, 24 og 48 h postoperatively PONV score 0, 6, 12, 24 and 48 h postoperatively Number of vomiting;Timepoint(s) of evaluation of this end point: 48 h postoperatively

Countries

Denmark

Contacts

Public ContactDepartment of Anesthesiology

Kolding Hospital

kjartan.eskjaer.hannig2@rsyd.dk4576360228

Outcome results

None listed

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