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NCT07737158
Venlafaxine for Non-specific Low Back Pain
Conditions: Non-specific Low Back Pain, Pain Management
Sex: All
Ages: 18 Years – 75 Years
Healthy volunteers: No
Phase: NA
Enrollment: 228
Sponsor: Beijing Tiantan Hospital
Location: Beijing Tiantan Hospital Beijing China
Summary
Chronic non-specific low back pain is the leading cause of productivity loss and disability worldwide, constituting a major public health challenge. This study aims to systematically evaluate and compare the role of the antidepressant drug Venlafaxine in chronic non-specific low back pain, which is of critical importance for optimising clinical practice and developing precise, individualised treatment regimens.
Eligibility Criteria
Inclusion Criteria:
* Adults aged 18 to 75 years.
* Diagnosis of chronic nonspecific low back pain, defined as pain located below the costal margin and above the inferior gluteal folds, lasting for more than 3 months, without a specific pathological cause.
* Moderate to severe pain, defined as a Numerical Rating Scale score of 3 or higher.
* Able to understand the study procedures and sign written informed consent.
Exclusion Criteria:
* Low back pain caused by a known specific pathological condition, including but not limited to fracture, malignancy, infection, inflammatory disease, or other identifiable structural or systemic causes.
* Major comorbidities that may interfere with study outcomes or represent contraindications to the study medication.
* Current or previous diagnosis of depression, regardless of whether treatment was received.
* Current or previous use of antidepressant medication.
* Current use of opioid analgesics.
* Pregnancy, breastfeeding, or planned pregnancy during the study period.
* Known allergy, hypersensitivity, or contraindication to toludesvenlafaxine.
* History of psychosis or other major psychiatric disorders.
* Any condition that, in the investigator's judgment, makes the participant unsuitable for the study.
Source: ClinicalTrials.gov (NCT07737158). StuddyBuddy aggregates publicly available trial information.