Actively Recruiting
The Influence of the Timing of Postoperative Rehabilitation Intervention on the Clinical Efficacy of Unilateral Biportal Endoscopic Spine System in the Treatment of Lumbar Disc Herniation
Led by Li Xiang · Updated on 2025-09-08
72
Participants Needed
1
Research Sites
104 weeks
Total Duration
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AI-Summary
What this Trial Is About
This study focuses on the impact of the timing of postoperative rehabilitation intervention on the clinical efficacy of unilateral biportal endoscopic spine surgery in the treatment of lumbar disc herniation. The main objective is to explore this impact and provide high-quality evidence-based medical evidence for making reasonable clinical decisions.
CONDITIONS
Official Title
The Influence of the Timing of Postoperative Rehabilitation Intervention on the Clinical Efficacy of Unilateral Biportal Endoscopic Spine System in the Treatment of Lumbar Disc Herniation
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Aged between 19 and 65 years.
- Diagnosed with lumbar disc herniation by imaging and scheduled for unilateral biportal endoscopic (UBE) surgery.
- Presenting with radicular pain in the lower extremity, with a history of less than 1 year.
- Able to understand Chinese and complete questionnaires independently.
- Physically capable of participating in exercise rehabilitation.
- Willing to participate and provide written informed consent.
You will not qualify if you...
- Aged under 18 or over 65 years.
- Combined with other spinal pathologies such as ankylosing spondylitis, rheumatoid arthritis, spinal tumor, spinal fracture, or cauda equina syndrome.
- Diagnosis of neurological disorders like multiple sclerosis or Parkinson's disease.
- Presence of uncontrolled cardiovascular, respiratory, or peripheral vascular diseases.
- History of severe psychiatric disorders such as schizophrenia.
- Previous history of spinal surgery.
- Pregnancy or lactation.
- Inability to understand or comply with the study procedures.
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Beijing Friendship Hospital
Beijing, Beijing Municipality, China, 100050
Actively Recruiting
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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