Interfacial Injection in Low Back Pain

Not Applicable

Completed

• Conditions: Low Back Pain
• Interventions: Procedure: interfacial injection; Procedure: physical therapy

• Registration Number: NCT05396508
• Lead Sponsor: Bursa Yüksek İhtisas Education and Research Hospital

Brief Summary

Its effect on thoracolumbar fascia and low back pain has been investigated in different studies.These studies suggest that the anatomical and histological features of the fascia may have an effect on low back pain. This study aimed to investigate the effectiveness of interfacial injection in patients with chronic back pain.

Detailed Description

Not available

Study Timeline

• Status Verified: 2019-03
• Study Start: 2019-04-01
• Primary Completion: 2022-01-01
• Study Completion: 2022-02-15
• Study First Submitted: 2022-05-25
• Study First Submitted QC: 2022-05-25
• Last Update Submitted: 2022-05-27
• Study First Posted: 2022-05-31
• Last Update Posted: 2022-06-02

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 61

Inclusion Criteria

• Low back pain for more than 6 months;
• Presence of MR findings radiologically diagnosing LDH;
• Numeric rating scale (NRS) > 5

Exclusion Criteria

• Spinal stenosis;
• Spondylolisthesis;
• Previous lumbar
• Spinal surgery

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
physical therapy + interfacial injection	interfacial injection	physical therapy + interfascial injection
physical therapy	physical therapy	physical therapy
physical therapy + interfacial injection	physical therapy	physical therapy + interfascial injection

Primary Outcome Measures

Name	Time	Method
NRS	6 month	Numeric rating scale(NRS) A numerical rating scale (NRS) requires the patient to rate their pain on a defined scale. For example, 0-10 where 0 is no pain and 10 is the worst pain imaginable

Secondary Outcome Measures

Name	Time	Method
ODI	6 month	Oswestry Disability Index Each topic category is followed by 6 statements describing different potential scenarios in the patient's life relating to the topic. The patient then checks the statement which most closely resembles their situation. Each question is scored on a scale of 0-5 with the first statement being zero and indicating the least amount of disability and the last statement is scored 5 indicating most severe disability.The scores for all questions answered are summed, then multiplied by two to obtain the index (range 0 to 100). Zero is equated with no disability and 100 is the maximum disability possible
NSAİD	6 month	The monthly consumption of NSAIDs was queried (pcs/month)

Trial Locations

Locations (1)

Bursa Yüksek İhtisas Eğitim ve Araştırma Hastanesi; 🇹🇷 Bursa, Turkey