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Evaluating the Effect of Dry Needling on the Radiating Pain in Subjects with Discopathic Low Back Pain

Evaluating the Effect of Dry Needling on the Radiating Pain in Subjects with Discopathic Low Back Pain

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015071121479N2
Enrollment
58
Registered
2015-08-31
Start date
2014-01-21
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

discopathy low back pain. Lumbar and other intervertebral disc disorders with radiculopathy

Interventions

Intervention 1: Participants in experimental group received standard physiotherapy for 10 sessions every other day and dry needling for 5 sessions. Standard physiotherapy included thermal modality, TE
Rehabilitation
Participants in experimental group received standard physiotherapy for 10 sessions every other day and dry needling for 5 sessions. Standard physiotherapy included thermal modality, TENS (Acupuncture
Subjects in control group received standard physiotherapy for 10 sessions every other day. Standard physiotherapy included thermal modality, TENS (Acupuncture like: Frequency = 1-4Hz, Duration= 250 ms

Sponsors

Isfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
74 Years to 44 Years

Inclusion criteria

Inclusion criteria: The inclusion criteria :( age between 20 and 50 years old ? radiating pain at one or both legs ? abnormal electromyographyfinding) exclusion: ( they had coagulation disorder or they were under anticoagulant therapy for any reason (due to high risk of hemorrhage following needling) ; if they suffered from psychologic disorders (due to unreliable pain report during the study) ; Subjects with needle phobia ; tumor and infection in lumbar region ; acute or chronic radiating LBP due to fracture or instability ; contraindications of dry needling )

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Radiating pain. Timepoint: at baseline (in the first intervention session), in the last intervention session and two months after the last intervention session (follow up). Method of measurement: visual analog scale.

Secondary

MeasureTime frame
Functional disability. Timepoint: at baseline (in the first intervention session), in the last intervention session and two months after the last intervention session (follow up). Method of measurement: Oswestry functional disability questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Abdolkarim Karimi

Isfahan University of Medical Sciences

a_karimi@rehab.mui.ac.ir00

Outcome results

None listed

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