Adalimumab on Preventing Post-chirurgic Recurrence on Crohn´s Disease

Sponsor
Grupo Espanol de Trabajo en Enfermedad de Crohn y Colitis Ulcerosa
Study ID
NCT01564823
Phase
PHASE3
Status
Completed

Conditions

  • Crohn´s Disease

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Metronidazole — DRUG
    Metronidazole: 250 mg/8h. 3 months.
  • Metronidazole — DRUG
    Metronidazole 250 mg/8h 3 months
  • Azathioprine — DRUG
    Azathioprine: 2.5 mg/kg of weight/day. 3 months.
  • Adalimumab — DRUG
    Adalimumab 160 mg then 80 mg. After 2 wk: 40 mg as maintenance.

Study Details

The present study objective is evaluate Adalimumab efficacy versus Azathioprine efficacy on prevention of endoscopic recurrence (Rutgeerts Index= 2b, 3 or 4) in Crohn´s Disease patients after 52 weeks of treatment.

Key Dates

Start date
Jun 30, 2012
Status verified
Mar 2015
Primary completion
Jan 31, 2015
Completion
Jan 31, 2015

Study Design

Enrollment
86 participants (actual)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT

Arms

  • Experimental: Metronidazole + Azathioprine.
    Metronidazole, oral intake. 250 mg/8h. 3 months. Azathioprine, 2.5 mg/weight kg/day, oral intake. All study.
  • Active Comparator: Metronidazole + Adalimumab
    Metronidazole Oral Intake. 250 mg/8h. During 3 months. Adalimumab Subcutaneous 160 mg and 80 mg 2wk. Then 40 mg during 2wk as maintenance.

Primary Outcome Measure

Number of endoscopic recurrences [ Time Frame: 52 weeks after the begin of the study ]