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Comparing the effect of acupuncture and medical treatment on subjective symptoms and neuromuscular electrophysiologic changes in patients with cervical disk herniation

Comparing the effect of acupuncture and medical treatment on subjective symptoms and Electromyography/Nerve Conduction Velocity (EMG/NCV) change in patients with cervical disk herniation

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015070311912N4
Enrollment
90
Registered
2015-11-13
Start date
2013-08-23
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

Cervical disc herniation. Cervical disc disorders

Interventions

Intervention 1: Intervention: acupuncture with 0.25*40 mm size needles on 20 acupoints , 3 times a week, each session 30 min for one month. Intervention 2: Control group: four different types of isome
Treatment - Drugs
Control group: four different types of isometric exercises plus 100 mg Celebrex tablets, twice daily (morning and night)

Sponsors

Vice Chancellor for Research, Mashhad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to No maximum

Inclusion criteria

Inclusion criteria: Major eligibility criteria: age older than 20 years old; confirmed diagnosis of cervical disc herniation; willing to participate in the study. Major exclusion criteria: polyneuritis or lesions of the cervical radicolopathy; hypothyroidism; multiple myeloma; amyloidosis; inability to perform daily functions individually; previous acupuncture treatment or surgery for cervical disc herniation; insulin dependent diabetes; pregnancy or less than 3 month post partum; epilepsy; cardiovascular disease; history of gastrointestinal disease and intolerance for NSAIDS; history of warfarin or heparin consumption or a hemorrhagic disease; definite indication for surgery based on rheumatologic consult and red and yellow flags.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Changes in electrodiagnostic tests (CMAP, DML, DSL, MNCV). Timepoint: Three months after the intervention. Method of measurement: Repeating the mentioned tests.

Secondary

MeasureTime frame
Clinical symptoms (neck, shoulder or arm pain, numbness and tingling). Timepoint: Three months after the end of intervention. Method of measurement: Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHosein Hasanabadi

Mashhad University of Medical Sciences

hasanabadih@mums.ac.ir+98 51 3802 2353

Outcome results

None listed

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