Recruiting

Anti-TNFα

Sponsor:

CHU de Quebec-Universite Laval

Code:

NCT02242474

Conditions

Rheumatoid Arthritis

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Interventions

Anti-TNF suspended perioperatively

Anti-TNFα continued perioperatively

Study Details

Brief summary:

Rheumatoid arthritis (RA) is a frequent inflammatory arthritis that can lead to severe joint deformity and often requires orthopaedic surgical interventions. Anti-Tumor Necrosis Factor α (anti-TNFα) are biological disease-modifying antirheumatic drugs (DMARDs) increasingly used in the treatment of rheumatoid arthritis. An increased risk of opportunistic infection was demonstrated in patients treated with those drugs. This observation led many national committees to recommend anti-TNFα suspension in the perioperative period to avoid a raise in the postoperative infection risk in those patients. This approach is not supported by the data available in the current literature and it exposes patients to an increased risk of inflammatory flare ups of their disease during and after anti-TNFα suspension, which can compromise their postoperative rehabilitation and their quality of life.

The objective of this prospective randomized multicentric trial is to determine the effect of anti-TNFα suspension in the perioperative period on the postoperative infection risk. Overall, 660 rheumatoid arthritis patients requiring an elective foot or ankle surgery will be randomized into two groups. In the first group, anti-TNFα will be stopped 3 half-lives before the surgery while they will be continued in the second group. The postoperative infection rate will be compared between the two groups. Postoperative complication rates, flares and revision surgeries as well as the functional improvement will be compared.

The study hypothesis is that there is no significant difference in the risk of postoperative infection between the two groups.

Results from this study will help determine the optimal way to use anti-TNFα in the perioperative period and will therefore improve the quality of life of rheumatoid arthritis patients.

Conditions

Rheumatoid Arthritis

Study ID

NCT02242474

Start date

Jul, 2015

Status verified date

Jul, 2018

Completion date

Oct, 2019

Anticipated

Primary completion date

Oct, 2019

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Inclusion Criteria:

  • Male and female 18 years of age or older
  • Rheumatoid arthritis diagnostic according to the American College Rheumatology (ACR) 1987 criteria \[38\]
  • Patient treated with anti-TNFα for at least six months
  • Elective unilateral surgery of the foot and ankle

Exclusion Criteria:

  • Patient unable to give informed consent
  • Surgery on an infected site
  • Severe distal peripheral vascular disease (no distal pulse)
  • Medical condition contraindicating surgery
  • Patient treated with biologic DMARD other than anti-TNFα
  • Circumstances preventing an adequate postoperative follow-up
  • Revision surgery

Study Design

Enrollment

660 participants

Anticipated

Allocation

Randomized

Intervention Model

Parallel Assignment

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

active comparator: Anti-TNF suspended perioperatively

Patients randomized to Group B will have their anti-TNFα therapy interrupted before surgery. Different authors suggested that anti-TNFα therapies should be suspended between two and five half-lives prior to surgery. In the current trial, anti-TNFα will be suspended three half-lives (± seven days) prior to surgery. All other medications used in the treatment of the disease (methotrexate, hydroxychloroquine, corticosteroid, etc.) will be documented and continued in the perioperative period. Non-steroidal anti-inflammatory drugs (NSAID) will be suspended seven days prior to surgery and will be restarted postoperatively. Anti-TNFα will be restarted once wound healing is completed.

experimental: Anti-TNFα continued perioperatively

Patients randomized to Group A will continue their anti-TNFα treatment unaltered during the whole perioperative period. Surgery will be performed without consideration in regards to the timing of the treatment. The time elapsed between the last anti-TNFα administration and the surgery will nonetheless be documented.

Interventions

Anti-TNF suspended perioperatively

Anti-TNFα continued perioperatively

Primary outcome measure

  • Surgical site infection [ Time Frame: Within one year after surgery ]

Central Contacts and Locations

Central contacts

Melissa Laflamme, MD, MSc

418-525-4444

Locations

Centre Hospitalier Universitaire de Québec

Recruiting

Québec, Quebec, Canada, G1V 2L9

Contacts

Melissa Laflamme, MD, MSc

418-525-4444

More Information

Sponsor

CHU de Quebec-Universite Laval

Last update posted

Jul 18, 2018

Last verified

Jul, 2018

Keywords

  • Rheumatoid arthritis
  • Surgical Wound Infection
  • Surgical Site Infection
  • Antirheumatic Agents
  • Perioperative Care
  • Anti-TNF
  • Anti-TNF-alpha

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by CHU de Quebec-Universite Laval on 2018-07-18.