Study of Autologous Conditioned Serum After Anterior Cruciate Ligament Reconstructive Surgery

Sponsor
University of Zagreb (Other)
Overall Status
Completed
CT.gov ID
NCT01037738
Collaborator
Croatian Institute of Health Insurance (Other)
62
1
2
32.1
1.9

Study Details

Study Description

Brief Summary

Abstract

Background

Pro-inflammatory cytokines play a pivotal role in osteoarthritis, as well as in bone tunnel widening after ACL reconstructive surgery. A new treatment option is to administer autologous conditioned serum (ACS) containing endogenous anti-inflammatory cytokines including IL-1Ra and growth factors (IGF-1, PDGF and TGF-ß1, among others) in the liquid blood phase.

Objective The purpose of this trial was to establish whether the osteoclastic effect could be affected by intra-articular application of ACS, thus resulting in a potential decrease of knee laxity and leading to a better postoperative outcome.

Methods In a prospective, randomized, double-blinded, placebo-controlled trial with two parallel groups, 62 patients were treated. Bone tunnel width was measured by CT scans, while clinical efficacy was assessed by patient-administered outcome instruments (WOMAC, IKDC 2000) up to one year following the ACL reconstruction in patients receiving either ACS (Group A) or placebo (Group B). The investigators compared the levels and dynamics of IL-1b concentrations in the synovial liquid and examined the correlation between the levels of IL-1b at three different post-operative points.

Level of evidence Therapeutic study, Level 1 (randomized controlled trial [significant differences and narrow confidence intervals])

Condition or Disease Intervention/Treatment Phase
  • Procedure: ACL reconstructive surgery and ACS/ Orthokin application
Phase 1

Study Design

Study Type:
Interventional
Actual Enrollment :
62 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Intraarticular Application of Autologous Conditioned Serum (ACS/Orthokine) Reduces Bone Tunnel Widening After ACL Reconstructive Surgery A Prospective, Randomized, Saline-controlled, Patient- and Observer-blinded, Parallel-design Trial
Study Start Date :
May 1, 2006
Actual Primary Completion Date :
Aug 1, 2008
Actual Study Completion Date :
Jan 1, 2009

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: ACS - Orthokin

Autologous conditioned serum (ACS) - Orthokin containing endogenous anti-inflammatory cytokines including IL-1Ra and growth factors (IGF-1, PDGF and TGF-ß1, among others) in the liquid blood phase.

Procedure: ACL reconstructive surgery and ACS/ Orthokin application
ACL reconstructive surgery and ACS/ Orthokin or Placebo intraarticular application on Day 0,1,6 and 10 postoperatively, regarding the Arm

Placebo Comparator: Placebo

Physiologic solution

Procedure: ACL reconstructive surgery and ACS/ Orthokin application
ACL reconstructive surgery and ACS/ Orthokin or Placebo intraarticular application on Day 0,1,6 and 10 postoperatively, regarding the Arm

Outcome Measures

Primary Outcome Measures

  1. Bone tunnel width - CT scans. Clinical efficacy - patient administered outcome instruments (WOMAC, IKDC 2000). [1 year]

Secondary Outcome Measures

  1. Measurements and correlation between the levels of synovial fluid IL-1b at three different post-operative points. [1 year]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
Eligible patients were:
  • older than 18 years

  • prior to each surgery, traumatic ACL rupture was determined on the basis of a clinical examination and confirmed by exploratory and therapeutic arthroscopic surgery in accordance with good surgical practice

  • the same preoperative diagnosis of isolated ACL rupture

  • a knee axis deviation up to 5°; knee osteoarthritis up to grade 1 according to the AO

  • knee chondral lesion up to grade 2 (Outerbridge classification).

Exclusion Criteria:
  • poor general health as judged by the orthopedic surgeon

  • Concomitant painful or disabling disease of the spine, hips, or lower limbs that would interfere with evaluation of the afflicted knee

  • Any clinically significant or symptomatic vascular or neurological disorder; crystalline, inflammatory and infectious arthropathies

  • Infections

  • Osteomyelitis

  • Alcohol/drug abuse

  • Known coagulopathy

  • Corticosteroid or anti-coagulant usage, and morbid obesity.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Medical School, University of Zagreb Zagreb Croatia 10000

Sponsors and Collaborators

  • University of Zagreb
  • Croatian Institute of Health Insurance

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
, ,
ClinicalTrials.gov Identifier:
NCT01037738
Other Study ID Numbers:
  • REC LCA 2B
First Posted:
Dec 23, 2009
Last Update Posted:
Dec 23, 2009
Last Verified:
Jan 1, 2009

Study Results

No Results Posted as of Dec 23, 2009