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A study of the efficacy of knee alcohol block for the treatment of knee arthrosis pain

A prospective study of the efficacy of anterior and posterior knee alcohol neurolysis for the treatment of knee osteoarthrosis pain

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
REBEC
Registry ID
RBR-2myky3
Enrollment
Unknown
Registered
2020-02-17
Start date
2019-02-04
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Gonarthrosis [knee arthrosis]

Interventions

Forty participants with chronic knee pain due to osteoarthritis will be submitted to ultrasound-guided genicular nerve block with 1 ml of 0.25% bupivacaine in 4 points to assess pain relief. If there
Drug
Procedure/surgery
E03.155.086.231

Sponsors

Universidade Federal de São Paulo
Lead Sponsor
Universidade Federal de São Paulo
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: Aged over 18 years. With knee pain for more than six months without improvement with clinical treatment and clinical and imaging diagnosis (radiography) of knee osteoarthritis with moderate pain intensity (pain greater than 4 by numerical scale).

Exclusion criteria

Exclusion criteria: Patients with cognitive impairment or psychiatric illness or other causes of knee pain (trauma; complex regional pain syndrome; prosthesis); infection at the puncture site; coagulopathy; anticoagulant use will be excluded.

Design outcomes

Primary

MeasureTime frame
Hope we have reduction of pain intensity,Patients will be assessed for pain intensity using a numerical scale from zero to 10 before the block and 15 days, 1, 3 and 6 months after the block; joint movement angle before the block and 1 and 6 months after the block; and WOMAC scale before the block and 15 days, 1, 3 and 6 months after the block.

Secondary

MeasureTime frame
Hope we have increased pain-free time, Patients will be assessed for pain intensity using a numerical scale from zero to 10 before the block and 15 days, 1, 3 and 6 months after the block; joint movement angle before the block and 1 and 6 months after the block; and WOMAC scale before the block and 15 days, 1, 3 and 6 months after the block.;A reduction in the use of rescue medications is expected, being assessed by the use of rescue in later assessments.

Countries

Brazil

Contacts

Public Contactgabriel;gabriel campi;campi

Unifesp;Unifesp

billxlv@hotmail.com;billxlv@hotmail.com55764848 voip 17006;55764848 voip 17006

Outcome results

None listed

Source: REBEC (via WHO ICTRP)