CClinicalTrials.gg
CompletedNCT00700297Updated Jun 18, 2008

Colchicine Randomized Double-Blind Controlled Crossover Study in Behcet's Disease

A Phase 2 interventional study of Colchicine and Placebo in Behcet's Syndrome, sponsored by Tehran University of Medical Sciences. Completed at 1 site in Iran, Islamic Republic of. Open to participants aged 14 Years to 60 Years. Per ClinicalTrials.gov, last updated 2008-06-18.

Sponsored by Tehran University of Medical Sciences · Phase 2, Interventional, and Treatment

Phase
Phase 2
Study type
Interventional
Enrollment
169
Allocation
Randomized
Ages
14 Years to 60 Years
Sex
All
01

Study summary

Colchicine was first used in Behcet's Disease (BD), in 1977. There are controversial reports of the efficacy of Colchicine in BD. For some experts the unresponsiveness of some patients could be explained by genetic difference between the Silk Road BD and sporadic BD from other parts of the world.

To test this hypothesis (the inefficacy of colchicine in the Silk Road BD), we designed a randomized double-blind controlled crossover study in Iran, which is in the middle of the Silk Road, and has the second highest prevalence of BD in the world.

Read the detailed description

Patients: They were selected as consecutive patients.

The entry criteria was: age between 14 and 60 years, confirmed diagnosis of Behcet's Disease, absence of major organ involvement (eye, brain, lung, and cardio-vascular involvement), having at least one active symptom, and no treatment for at least one month. Patients were explained the study design and they gave a signed written consent. During the two phases of study, if a major organ involvement appeared, the patient was moved out of the study. All patients fulfilled the new International Criteria for Behcet's Disease.

Method: patients were randomized at the study entry to take either colchicine or placebo. At 4 months, they were crossed over. Those who were taking colchicine went on placebo and those on placebo went on colchicine. Each patient tried therefore, both colchicine and placebo. The primary outcome was the effect of colchicine on the disease activity index, the IBDDAM (16-17). To calculate the overall IBDDAM of the baseline, the IBDDAM of the last 12 months (prior to the study) of each manifestation was calculated and added together. The overall disease activity index was then divided to the number of months (12 months) to have the mean activity index per month. IBDDAM was then measured every 2 months (in the middle and at the end, in each arm of the study). The total IBBDAM of the 4 months was then divided by 4 to have the mean activity index per month. The secondary outcome was to see how the individual symptoms responded to colchicine (IBDDAM of each manifestation).

Statistical analysis: The analysis was done by the intention to treat method. As the difference between IBDDAM before and after treatment had normal distribution Student T test for paired samples were used to evaluate the outcome in the colchicine and the placebo group. As the Levene's test showed the homogeneity of variance, ANOVA (one way) was used to test the effect of treatment (colchicine and placebo) and gender on patients' outcome. The dependent variable was the difference between IBDDAM (before and after the treatment). The independent variables were the treatment, and the gender. SPSS 15 was used for all statistical calculations.

02

Conditions studied

  • Behcet's Syndrome

Browse trials for

Keywords

  • Oral aphthosis
  • Genital aphthosis
  • Psuedofolliculitis
  • Erythem nodusom
  • Joint manifestations
  • Colchicine
03

In context

Behcet Syndrome

136 studies on the registry are indexed under Behcet Syndrome; 43 are open to participants now.

This study's enrollment of 169 is above the median of 50 across 70 interventional studies indexed under Behcet Syndrome.

Browse Behcet Syndrome studies →

Lead sponsor

Tehran University of Medical Sciences is the lead sponsor of 227 studies on the registry; 12 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
14 Years to 60 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Patient's who fulfilled the International Criteria for Behcet's Disease.

Exclusion criteria

Exclusion Criteria:

  • major organ involvement
  • Hypersensitivity reaction
05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Crossover assignment
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
169 participants (actual)

Study arms

  • Active comparator
    Colchicine

    Patients who received Colchicine and went on placebo after 4 months

    Drug: Colchicine

  • Placebo comparator
    Placebo

    Patients who received placebo and went on Colchicine after 4 months

    Drug: Placebo

Interventions

  • DrugColchicine

    100 mg Colchicine per day for 4 months

    Also known as: Modacine

  • DrugPlacebo

    One tablet placebo per day for 4 months

06

What researchers measure

Primary outcomes

  1. Iranian Behcet's Disease Dynamic Activity Measurement (IBDDAM)

    Time frame: 8 months

Secondary outcomes

  1. Oral Aphthosis

    Time frame: 8 months

  2. Genital Aphthosis

    Time frame: 8 months

  3. Psuedofolliculitis

    Time frame: 8 months

  4. Erythem Nodusom

    Time frame: 8 months

  5. Joint Manifestations

    Time frame: 8 months

07

Study locations

1 site
  • Rheumatology research Center, Tehran UMS
    Tehran, 14114, Iran, Islamic Republic of
08

References and documents

Publications

  • Davatchi F, Shams H, Rezaipoor M, Sadeghi-Abdollahi B, Shahram F, Nadji A, Chams-Davatchi C, Akhlaghi M, Faezi T, Naderi N. Rituximab in intractable ocular lesions of Behcet's disease; randomized single-blind control study (pilot study). Int J Rheum Dis. 2010 Aug;13(3):246-52. doi: 10.1111/j.1756-185X.2010.01546.x. PubMed 20704622 ↗
  • Davatchi F, Sadeghi Abdollahi B, Tehrani Banihashemi A, Shahram F, Nadji A, Shams H, Chams-Davatchi C. Colchicine versus placebo in Behcet's disease: randomized, double-blind, controlled crossover trial. Mod Rheumatol. 2009;19(5):542-9. doi: 10.1007/s10165-009-0200-2. Epub 2009 Jul 14. PubMed 19597921 ↗
09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 18, 2008, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT00700297
Lead sponsor
Tehran University of Medical Sciences
First posted
Jun 18, 2008
Start date
Aug 2002
Primary completion
Oct 2005
Completion
May 2006
Last update
Jun 18, 2008

Study contacts

Fereydoun Davatchi, Professor
study chair · Rheumatology Research Center, Tehran University for Medical Sciences
Bahar Sadeghi, MD
principal investigator · Rheumatology research Center, Tehran University for Medical Sciences
Arash Tehrani Banihashemi, MD, MPH
principal investigator · Rheumatology Research Center, Tehran University for Mrdical Sciences
Farhad Shahram, Professor
principal investigator · Rheumatology Research Center, Tehran University for Medical Sciences

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in May 2008. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion