Effect of caudal-epidural analgesia in back pain

Comparison of two caudal-epidural methods and regional myofascial injection in patients with back pain

Status

Recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20241017063397N1

Enrollment

Registered

2024-12-15

Start date

2024-12-21

Completion date

Unknown

Last updated

2025-01-08

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

Conditions

BACK PAIN. Other reaction to spinal and lumbar puncture

Interventions

Intervention group: Women and men with myofascial pain syndrome in low back pain.

Eligibility

Sex/Gender

All

Age

20 Years to 75 Years

Inclusion criteria

Inclusion criteria: Women and men with myofascial pain syndrome in back pain aged 20 to 75 years

Exclusion criteria

Exclusion criteria: People with diabetes, heart failure, blood pressure, skin diseases, back surgery, seizures and drug addiction

Design outcomes

Primary

Measure	Time frame
Low back pain. Timepoint: 6 WEEKS. Method of measurement: VAS.	—

Secondary

Measure	Time frame
VAS score. Timepoint: 6 weak. Method of measurement: Questionnaire.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMaryam Nasoohi

Shahid Beheshti University of Medical Sciences

nasoohi_m@yahoo.com+98 21 2209 1492

Outcome results

None listed

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