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NCT07263737
Pulsed Electromagnetic Field Therapy for Neuropathic Pain in Lumbar Disc Herniation
NA trial testing Pulsed electromagnetic field (PEMF) in Lumbar Disc Herniation With Radiculopathy in 46 participants. Completed in 15 August 2023.
15 July 2023
Quick facts
| Lead sponsor | Haydarpasa Numune Training and Research Hospital |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | quadruple |
| Primary purpose | treatment |
| Enrollment | 46 |
| Start date | 30 October 2022 |
| Primary completion | 15 July 2023 |
| Estimated completion | 15 August 2023 |
| Sites | 1 location across Turkey (Türkiye) |
Drugs / interventions tested
- Pulsed electromagnetic field (PEMF)
- Sham PEMF
Conditions studied
- Lumbar Disc Herniation With Radiculopathy — all drugs for Lumbar Disc Herniation With Radiculopathy →
Sponsor
Haydarpasa Numune Training and Research Hospital
Who can join
Adults 18 to 75, any sex, with Lumbar Disc Herniation With Radiculopathy. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
This randomized controlled study evaluated whether adding pulsed electromagnetic field (PEMF) therapy to conventional physical therapy provides additional benefits for neuropathic pain and disability in patients with lumbar disc herniation (LDH). → This study randomly assigned patients into groups to compare treatments. It examined whether adding pulsed electromagnetic field (PEMF) therapy to standard physical therapy could give extra improvement in nerve-related pain and daily function in people with a slipped disc in the lower back. Fifty-two patients with ≥3 months of radicular and neuropathic symptoms were enrolled and randomly assigned to a treatment group (PEMF + conventional therapy) or a control group (sham PEMF + conventional therapy). → Fifty-two patients who had leg pain and nerve-related symptoms for at least three months joined the study. They were randomly placed into either a treatment group (which received PEMF plus regular therapy) or a control group (which received a fake PEMF treatment plus regular therapy). Both groups received transcutaneous electrical nerve stimulation, hot packs, and a lumbar exercise program for 15 sessions. → Both groups also received the same standard treatments: electrical nerve stimulation, hot packs, and a lower-back exercise program for 15 sessions. Clinical outcomes-including Visual Analog Scale (VAS), pressure pain threshold, Modified Schober test, DN4, PainDetect, Oswestry Disability Index (ODI), and SF-36-were assessed at baseline, post-treatment, and one month after treatment. → Several health measures were checked before treatment, right after treatment, and again one month later. These included pain level (VAS), how sensitive the area was to pressure, lower-back flexibility, nerve-pain questionnaires (DN4 and PainDetect), disability level (ODI), and overall quality of life (SF-36). Forty-six patients completed the study. → A total of 46 patients finished the study. Both groups showed significant improvements in VAS scores, neuropathic pain questionnaires (DN4, PainDetect), ODI, and several SF-36 subscales (physical functioning, role-physical, and pain), with additional improvements in emotional role and social functioning observed only in the PEMF group. → Both groups improved in many areas: pain levels, nerve-pain scores, disability, and some parts of quality of life (such as physical functioning, daily roles, and pain). Only the PEMF group showed extra improvement in emotional well-being and social activities. However, none of the between-group comparisons demonstrated significant differences. * However, when the two groups were compared to each other, there were no meaningful differences. No meaningful changes were found in lumbar flexibility or pressure pain thresholds in either group. → Neither group showed important changes in lower-back flexibility or in how much pressure they could tolerate on painful areas. In conclusion, adding PEMF therapy to conventional physical therapy did not provide additional benefit for neuropathic symptoms, radicular pain, disability, lumbar flexibility, pressure pain threshold, or quality of life in patients with LDH-related neuropathic pain. → In summary, adding PEMF therapy to regular physical therapy did not give extra benefits for nerve pain, leg pain, disability, back flexibility, sensitivity to pressure, or quality of life in people with nerve-related pain caused by a slipped disc.
Publications & conference data
No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.
Verify or expand the search:
- PubMed search for NCT07263737
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT07263737 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Haydarpasa Numune Training and Research Hospital
- Last refreshed: 18 February 2026
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07263737.
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