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RECRUITING
NCT07709416
NA

Toludesvenlafaxine for Non-specific Low Back Pain

Sponsor: Beijing Tiantan Hospital

View on ClinicalTrials.gov

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 toludesvenlafaxine in chronic non-specific low back pain, which is of critical importance for optimising clinical practice and developing precise, individualised treatment regimens.

Official title: Efficacy and Safety of Toludesvenlafaxine in the Treatment of Non-specific Low Back Pain

Key Details

Gender

All

Age Range

18 Years - 75 Years

Study Type

INTERVENTIONAL

Enrollment

132

Start Date

2026-07-15

Completion Date

2028-12-01

Last Updated

2026-07-27

Healthy Volunteers

No

Interventions

DRUG

Active Comparator #1

Participants in the control group will receive routine clinical care for chronic nonspecific low back pain.

DRUG

Toludesvenlafaxine

Participants in the toludesvenlafaxine group will receive oral toludesvenlafaxine in addition to background care. Toludesvenlafaxine will be administered at 80 mg once daily. For participants with insufficient pain relief and acceptable tolerability, the dose may be cautiously increased to 160 mg once daily. The maintenance treatment period will be 3 months.

Locations (1)

Fang Luo

Beijing, China