Skip to main content
OpenTrials
Recruiting

NCT Number: NCT06902805

Efficacy of Two Ultrasound-guided Intra-articular Injections of Botox® Combined With Custom-made Rigid Splinting in Painful Base-of-thumb Osteoarthritis.

The main objective of this study will be to compare the effects of 2 intra-articular injections of onabotulinumtoxinA with those of 1 intra-articular injection of onabotulinumtoxinA and 1 of normal saline and those of 2 intra-articular injections of normal saline on base-of-thumb pain at 6 months after the first injection.

Recruiting

Interested in participating?

Request Info

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2 / Phase 3

Primary location

Assistance Publique - Hôpitaux de Paris, Service de Rééducation et de Réadaptation de l'Appareil Locomoteur et des Pathologies du Rachis du Pr François Rannou, Hôpital Cochin

Paris, Île-de-France Region, 75014, France

Location status: Recruiting

Location contact

Christelle Nguyen, MD, PhD

CONTACT

[email protected]

01 58 41 29 45 ext. +33

About this study

The base of the thumb is a frequent location of osteoarthritis. Base-of-thumb osteoarthritis affects middle-aged and older individuals and results in base-of-thumb pain and limitations in hand-specific activities. For the medium and long term, evidence suggests that splinting could reduce pain and improve hand function. For the short term, a combination of conservative treatments is recommended, with small-to-moderate treatment effect. However, use of intra-articular treatments (e.g., glucocorticoids and hyaluronan) for the short and medium term is currently debated. Use of intra-articular botulinum toxin A injection as a pain modulator in joint diseases has recently raised interest. Botulinum toxin A is a neurotoxin produced by Clostridium botulinum that inhibits acetylcholine release into the synaptic cleft in cholinergic nerve terminals. Additionally, treatment with botulinum toxin A showed intrinsic antinociceptive effects in various animal models of joint diseases.

In a pilot single-centred randomized controlled trial of 60 participants with painful base-of-thumb osteoarthritis, the investigators compared the effects of a single intra-articular injection of onabotulinumtoxinA (Botox® ) with those of a single intra-articular injection of normal saline on base-of-thumb pain, and found a significant reduction in pain.

Several perspectives raised from this pilot study. Like in the treatment of spasticity, repeated courses of intra-articular injections onabotulinumtoxinA may be necessary to obtain sustained analgesic effects over time. A replication of these findings in a multicentred setting, analysis of cost-effectiveness and description of safety at longer term are also needed before the official recommendation of this treatment. In RHIBOT II, the investigators hypothesize that 2 ultrasound-guided intra-articular injections of onabotulinumtoxinA, as an add-on therapy to custom-made rigid splinting, could reduce base-of-thumb pain at 6 months after the first injection.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • • Individuals aged at least 18 years;
  • Pain intensity of at least 30 on a self-administered 11-point pain numeric rating scale (0: no pain to 100: maximal pain);
  • Pain involving the base of the thumb;
  • X-ray evidence of trapezometacarpial osteoarthritis with at least two of the following items involving the trapezometacarpial joint: osteophytes, joint space narrowing, subchondral bone sclerosis, or subchondral cysts;
  • 1990 ACR classification criteria for hand osteoarthritis adapted to trapezometacarpial osteoarthritis.
  • Patient able to give written informed consent prior to participation in the study
  • Affiliation with a mode of social security (profit or being entitled).
  • Negative pregnancy test in women of childbearing potential

Exclusion criteria

  • • Secondary osteoarthritis;
  • History of thumb surgery, inflammatory or crystal-associated rheumatic disease, or epilepsy;
  • Uncontrolled dysphagia, pneumonia, cardiovascular diseases, or clinical or subclinical signs of neuromuscular transmission disorders;
  • Contra-indication to onabotulinumtoxinA;
  • Neurological disorders involving the hands other than carpal tunnel syndrome;
  • Collagen disorders involving the hands;
  • Osteoarthritis predominating at the scaphotrapezial joint on x-ray;
  • Bilateral trapezometacarpial osteoarthritis without a predominant painful side;
  • Hand or wrist trauma for up to 2 months;
  • Intra-articular treatments for up to 2 months;
  • Use of IM, IV or oral corticosteroids for up to 2 months.
  • Protected adults (including individual under guardianship by court order)
  • Pregnant women and lactation; lack of contraception for women of childbearing potential
  • Patient participating in another investigational therapeutic study
  • Patient unable to speak and read french

Treatment and study plan

OnabotulinumtoxinA

Drug

intra-articular injection

Normal saline (placebo)

Drug

intra-articular injection

Primary outcomes

  1. Base-of-thumb pain on a self-administered 11-point numeric rating scale

    Time frame: 6 months

    French version of the self-administered base-of-thumb pain numeric rating scale (0: no pain to 100: maximal pain)

Secondary outcomes

  1. Base-of-thumb pain on a self-administered 11-point numeric rating scale

    Time frame: 1 and 12 months

    French version of the self-administered base-of-thumb pain numeric rating scale (0: no pain to 100: maximal pain)

  2. Hand-specific activity limitations on the self-administered Cochin Hand Function Scale

    Time frame: 6 and 12 months

    mean change from baseline in hand-specific activity limitations in the previous 2 weeks on the self-administered Cochin Hand Function Scale (0: no limitations to 90: maximal limitations) at 6 and 12 months

  3. patient global assessment on a self-administered 11-point numeric rating scale

    Time frame: 6 and 12 months

    mean change from baseline in patient global assessment on a self-administered 11-point numeric rating scale (0: worst possible condition to 100: best possible condition) at 6 and 12 months

  4. health-related quality of life on the self-administered EQ-5D-5L questionnaire

    Time frame: 6 and 12 months

    mean change from baseline in health-related quality of life on the self-administered EQ-5D-5L questionnaire (0: death, 1: best quality of life) at 6 and 12 months

  5. Osteoarthritis Research Society International-Outcome Measures in Rheumatology response

    Time frame: 6 and 12 months

    Osteoarthritis Research Society International-Outcome Measures in Rheumatology response (Response / No response)

  6. estimated total costs and incremental cost-utility ratio

    Time frame: 12 months

Study contacts

Contact information is provided by the study sponsor or research team.

Christelle NGUYEN, MD, PhD

CONTACT

[email protected]

01 58 41 29 45 ext. +33

Laetitia PEAUDECERF, PhD

CONTACT

[email protected]

01 58 41 12 13 ext. +33

Sponsors and collaborators

Lead sponsor

Assistance Publique - Hôpitaux de Paris

Other

Collaborators

  • URC-CIC Paris Descartes Necker Cochin

Registry information

Official study title

Medium-and Long-term Efficacy of Two Ultrasound-guided Intra-articular Injections of onabotulinumtoxinA (Botox®) Combined With Custom-made Rigid Splinting in Painful Base-of-thumb Osteoarthritis : a Randomized Double-blind Controlled Trial in Three-parallel Arms

Acronym: RHIBOTII

Important dates

Study start
2025
Primary completion
2027
Study completion
2028
First posted
Mar 30, 2025
Registry last updated
Apr 3, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.