The patient-reported outcome of postoperative Prostaglandin E1 derivative in Lumbar spine surgery: a randomized, double-blinded, controlled trial

Phase 4

• Conditions: Postoperative leg numbness; Prostaglandin E1 derivative; Lumbar spine surgery; Postoperative outcome; Patient reported outcome

• Registration Number: TCTR20201010003
• Lead Sponsor: /A

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2020-10-10
• Study Completion: 2022-12-31
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Pending (Not yet recruiting)
• Sex: All
• Target Recruitment: 60

Inclusion Criteria

1.Degenerative lumbar spine disease patients
2.patients who have to undergo lumbar spine surgery (1-2 levels)
3.leg numbness confirmed by Semmes-Weinstein monofilament test
4.age 18-70 years

Exclusion Criteria

1.patients with Lumbar spine disease not caused by denerative disease
2.patients with history of previous Lumbar spine surgery
3.Patients with peripheral vascular disease
4.Pregnancy or Breastfeeding patients
5.Patients who cannot be regular followed up

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
eg numbness 12 week Visual analog scale

Secondary Outcome Measures

Name	Time	Method
Back pain, leg pain 12 week Visual analog scale