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Comparison the of effects Magnesium Sulfate and triamcinolone as Adjuvants with Ropivacaine for caudal block in Low Back Pain

Comparison the of effects Magnesium Sulfate and triamcinolone as Adjuvants with Ropivacaine for caudal block in Low Back Pain

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20230502058054N1
Enrollment
40
Registered
2023-07-18
Start date
2023-07-23
Completion date
Unknown
Last updated
2023-07-25

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

Conditions

Patients with low back pain who have spinal canal stenosis or several disc bulging or protrusion or degeneration changes in MRI. low back with sciatica

Interventions

Intervention 1: Intervention group: Magnesium Sulfate. Intervention 2: Intervention group: Triamcinolone.

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 60 Years

Inclusion criteria

Inclusion criteria: All patients with low back pain who have had canal stenosis, multiple disc herniation or multiple degenerative joint disease(based on MRI report), with at least 3 months pain and non responsive to conservative treatments such as physiotherapy with pain score of at least 4 between 30-60 years old.

Exclusion criteria

Exclusion criteria: Patients with :1-epidural steroid injection during last 3 months, without previous MRI report.2- coagulation disorders 3- pregnant 4- women with milk feeding 5- sensitivity to radiology contrast medications 5- patients with psychological disease 6- unstable hydrodynamic status. 7- previous back surgery 8- contraindication for local anesthetic drugs.9- infection 10- Allergy to medications( local anesthetic, steroid or magnesium) 11- unwillingness of patients to study 12- patients who do not sign inform consent.

Design outcomes

Primary

MeasureTime frame
Comparison of magnesium sulfate and triamcinolone as adjuvant with ropivacaine for caudal block on pain score in patients with low back pain. Timepoint: Preblock and 1 and 3 month after block. Method of measurement: numeric rating scale.

Secondary

MeasureTime frame
Modified Oswestry disability questionnaire score. Timepoint: Preblock and 1 and 3 month after block. Method of measurement: Questionnaire score.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactPayman ?Dadkhah

Shahid Beheshti University of Medical Sciences

pdadkhah@sbmu.ac.ir+98 21 7758 3043

Outcome results

None listed

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