Colchicine as Treatment for People With Hand Osteoarthritis

Phase 4

Completed

• Conditions: Osteoarthritis Finger; Osteoarthritis Hand
• Interventions: Drug: Colchicine 0.5 MG; Drug: Placebo

• Registration Number: NCT04601883
• Lead Sponsor: Henning Bliddal

Brief Summary

The study aims to compare oral colchicine 0.5 mg administered two times daily for 12 weeks with placebo as a treatment of hand OA symptoms.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2020-10-12
• Study First Submitted QC: 2020-10-20
• Study First Posted: 2020-10-26
• Study Start: 2021-01-15
• Primary Completion: 2022-08-03
• Study Completion: 2022-08-03
• Status Verified: 2023-02
• Last Update Submitted: 2023-02-14
• Last Update Posted: 2023-02-15

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 100

Inclusion Criteria

1. Age ≥18 years.
2. Hand OA according to the ACR criteria above.
3. Hand OA finger pain: Pain at rest ≥40 mm on VAS (0 to 100 mm range).

Exclusion Criteria

Comorbidities

1. Other known medical disease that may affect joints, e.g. RA, gout, PsA

2. Positive anti-cyclic citrullinated peptide (>10 kU/L)

3. Known cutaneous deposition diseases (e.g. amyloidosis or porphyria).

4. Known blood dyscrasias and coagulation disorders

5. Known malignancy (except successfully treated squamous or basal cell skin carcinoma)

6. Elevated alanine transaminase (>45 U/L females, >70 U/L for males)

7. Creatinine clearance ≤60 ml/min

8. Elevated creatine kinase (>210 U/L females, >280 U/L for males)

9. Known allergies towards the interventions

10. Drug or alcohol abuse in the last year

11. Generalised pain syndromes such as fibromyalgia

12. Current reflux

13. Current or recurrent diarrhoeal illnesses

14. Current abdominal pain

15. Known peripheral neuropathies

16. Any other condition or impairment that, in the opinion of the investigator, makes a potential participant unsuitable for participation or which obstruct participation, such as e.g. psychiatric disorders.

    Medical history

17. History of hand surgery within 12 months prior enrolment.

18. History of arthroplasty or arthrodesis in the hand Management strategies

19. Treatment with P-glycoprotein inhibitors and/or cytochrome P450 3A4 (CYP3A4) inhibitors, see section "Colchicine safety in drug-drug interactions" and table 7. If potential participants have been treated with these pharmaceuticals previously, treatment must be terminated 5 half-lifes before initiation of study drug.

20. Use of systemic corticosteroids equivalent of ≥ 7.5 mg prednisolone daily within 3 months.

21. Participation in experimental device or experimental drug study 3 months prior to enrolment.

22. Intra-articular treatments or aspirations of any kind of any joint in the hands 3 months before inclusion

23. Intra-articular corticosteroids into any joint 1 months before inclusion

24. Current use of synthetic or non-synthetic opioids

25. Scheduled surgery during study participation

26. Planning to start other treatment for hand OA in the study participation period.

    Reproductive system

27. Pregnancy.

28. Planned pregnancy within the study period, 3 months after end of study treatment for female fertile participant and 6 months after end of study treatment for male participant.

29. Insufficient anti-conception therapy for female fertile participants within the study period and 3 months after end of study treatment. Sufficient anti-conception therapy consists of intra-uterine device (coil),hormonal anti-conception (birth control pills, implant, intra-uterine system, dermal patch, vaginal ring, or injections) or sexual abstinence Female participants are considered infertile if they are postmenopausal or if they have undergone surgical sterilisation (bilateral salpingectomy, hysterectomy or bilateral oophorectomy). Postmenopausal state is defined as no menses for 12 months without alternative medical cause before inclusion in the study. Menopause state will be confirmed by measurement of follicle stimulating hormone.

30. Insufficient anti-conception therapy for male participants within the study period and 6 months after end of study treatment. Sufficient anti-conception therapy consists of condom or sexual abstinence. Male participants are considered sterile if they have undergone surgical sterilisation (vasectomy).

31. Breast-feeding

A target hand will be selected for outcome assessment once individual fulfills in- and exclusions criterias. Selection of the target hand will adhere to the following, with advancement to next step if unable to choose target hand based on the given criteria.

1. The hand with most overall pain, assessed by VAS finger joint pain.
2. The hand with most overall reduced function, assessed by AUSCAN function subscale.
3. The hand with most overall stiffness, assessed by AUSCAN stiffness subscale.
4. The hand with most swollen joints, assessed by physician joint count.
5. The hand with most tender joints, assessed by physician joint count.
6. The hand with highest summed radiographic score, assessed by radiographic scoring of conventional X-ray.
7. If unable to select target hand based on the above criteria, a target hand will be randomly assigned.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Colchicine	Colchicine 0.5 MG	Tablet colchicine 0.5 mg administered two times daily
Placebo	Placebo	Tablet placebo administered two times daily

Primary Outcome Measures

Name	Time	Method
Finger pain	Week 12	To compare the effect of oral colchicine 0.5 mg bid, relative to placebo, on changes in finger joint pain of the target hand from baseline to week 12, in patients with painful hand OA measured on a visual analogue scale spanning from 0 to 100, where 0 equals no symptoms and 100 equals worst imaginable symptoms.

Secondary Outcome Measures

Name	Time	Method
Function	Week 12	To compare the effect of oral colchicine 0.5 mg bid, relative to placebo, from baseline to week 12, in patients with painful hand OA on changes in function of both hands measured on the Australian/Canadian Hand Index Function Score spanning from 0 to 900, where higher scores equals worse function.
Thumb base pain	Week 12	To compare the effect of oral colchicine 0.5 mg bid, relative to placebo, from baseline to week 12, in patients with painful hand OA on changes in thumb base pain of the target hand measured on a visual analogue scale spanning from 0 to 100, where 0 equals no symptoms and 100 equals worst imaginable symptoms.
Pain hands	Week 12	To compare the effect of oral colchicine 0.5 mg bid, relative to placebo, from baseline to week 12, in patients with painful hand OA on changes in pain of both hands measured on the Australian/Canadian Hand Index Pain Score spanning from 0 to 500, where higher scores equals worse pain.
Joint activity	Week 12	To compare the effect of oral colchicine 0.5 mg bid, relative to placebo, from baseline to week 12, in patients with painful hand OA on changes in joint activity of the target hand measured on physician tender joint count
Patient global assessment	Week 12	To compare the effect of oral colchicine 0.5 mg bid, relative to placebo, from baseline to week 12, in patients with painful hand OA on changes in patient global assessment measured on a visual analogue scale spanning from 0 to 100, where 0 equals no symptoms and 100 equals worst imaginable symptoms.
Quality of life measured by European Quality of Life 5 Dimensions	Week 12	To compare the effect of oral colchicine 0.5 mg bid, relative to placebo, from baseline to week 12, in patients with painful hand OA on changes in quality of life measured on the European Quality of Life 5 Dimensions spanning from -0.624 to 1.000, where higher scores equals better quality of life.
Hand strength	Week 12	To compare the effect of oral colchicine 0.5 mg bid, relative to placebo, from baseline to week 12, in patients with painful hand OA on changes in hand strength of the target hand measured on grippit
Number of treatment responders according to OMERACT-OARSI response criteria	Week 12	The following two conditions is observed at the post-baseline assessment: 1. In either pain (finger pain) or function (function), a high improvement in the subscale, where high improvement in a subscale is achieved if there is both a \> 50% improvement from Baseline and an absolute change from Baseline of \> 20 percent points (0-100 scale), OR; 2. Improvement in at least two of the following three: * Improvement in pain (finger pain) defined as \> 20% improvement from Baseline and an absolute change from Baseline of \> 10 points (0-100 scale); * Improvement in function (function) defined as \> 20% improvement from Baseline and an absolute change from Baseline of \> 10 points (0-100 scale); * Improvement in patient's global assessment defined as \> 20% improvement from Baseline and an absolute change from Baseline of \> 10 mm (0-100 scale)

Trial Locations

Locations (1)

The Parker Institute, Bispebjerg and Frederiksberg Hospital; 🇩🇰 Copenhagen, DK, Denmark