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

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age19-65
SponsorLi Xiang

About this trial

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.

Eligibility criteria

Qualifiers

Aged between 19 and 65 years.

Disqualifiers

Aged under 18 or over 65 years.

Trial design

Treatments tested in this trial

  • Standardized Postoperative Rehabilitation Protocol

Treatment groups

72 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Li Xiang

Lead sponsor

Beijing Friendship Hospital

Sponsor institution