Sacroiliac joint syndrome: Surgical and clinical comparative examinations to effectiveness and security of the SIJ Fusio

• Conditions: M19.05; M99.84

• Registration Number: DRKS00021203
• Lead Sponsor: Paracelsus-Klinik Schöneck Wirbelsäulenchirurgie/ Neurotraumatologie

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Completion: 2019-12-30
• Study Start: 2020-04-08
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 51

Inclusion Criteria

Patients male and female aged> 18 years; Previous conservative treatment with insufficient success; Positive results after intra-articular injections of local anesthetics; Positive decision on the surgical intervention by the treating doctor and by the patient

Exclusion Criteria

Manifest osteoporosis; Women of childbearing age without adequate contraceptive protection; Pregnant women; Contraindication to anesthesia; Immature patients or patients with insufficient compliance

Study & Design

• Study Type: observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
patient's opinion regarding their satisfaction with the treatment result 6 months after the Surgery in comparison for both iFuse implants.

Secondary Outcome Measures

Name	Time	Method
pain severity (VAS) follow-up examinations after 6 weeks, after 6 months and additionally for the closed cases after 12, 24 and 36 months; functional ability (Oswestry Score) to the above times; patients`s opinion on the above times