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Comparison between infiltration with Hyaluronic Acid and Corticosteroid in the joint in the treatment of chronic low back pain: clinical study

Comparative study between Hyaluronic Acid and Corticosteroids in facet joints in the treatment of chronic low back pain: randomized clinical study

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
REBEC
Registry ID
RBR-8qcgzxw
Enrollment
Unknown
Registered
2024-09-03
Start date
2025-05-01
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

Musculoskeletal Pain

Interventions

This is a two-arm, double-blind, randomized controlled clinical study. Experimental group: 21 patients will undergo infiltration of 1% hyaluronic acid (single injection) 1ml in each joint. Dilution of
E03.155.086.231

Sponsors

Hospital e Maternidade São Domingos
Lead Sponsor
Hospital e Maternidade São Domingos
Collaborator

Eligibility

Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Both genders; older than 18 years; with chronic low back pain for more than 3 months; with pain intensity greater than 4 on the visual analogue pain scale; no radicular pain; caused by degeneration of the facet joint and which presents relief after test block

Exclusion criteria

Exclusion criteria: Trauma patients; neurological deficits; infection at the puncture site; cognitive impairment; psychiatric illness; hypersensitivity to medications; use of anticoagulants; coagulopathy and pregnant women will be excluded

Design outcomes

Primary

MeasureTime frame
Reduction in pain intensity after hyaluronic acid injection in patients with chronic low back pain due to facet joint degeneration

Secondary

MeasureTime frame
Reduced use of complementary analgesics, Improved functional capacity and Improved quality of life

Countries

Brazil

Contacts

Public ContactJosé Alberto Pires

Universidade Federal do Maranhão

medalbertopires@uol.com.br+55 (98) 992401999

Outcome results

None listed

Source: REBEC (via WHO ICTRP)