Effect and Safety of Local Injection of Botulinum Toxin Type B Against Digital Ulcer in Systemic Sclerosis

Gunma University

Status and phase: Completed; Phase 2

Conditions: Systemic Sclerosis Patients With Digital Ulcers

Treatments: Drug: Botulinum toxin type B (2500 units / vial); Drug: Physiological saline

Study type: Interventional

Funder types: Other

Identifiers

NCT03007004

D2016017

Details and patient eligibility

About

Efficacy and safety of local infusion of botulinum toxin type B in patients with systemic sclerosis (SSc) with digital ulcer is evaluated by a randomized, double-blind study.

Full description

To assess the efficacy and safety of local injection of botulinum toxin type B (BTX-B) against digital ulcers (DUs) and Raynaud's phenomenon (RP) in patients with systemic sclerosis (SSc).

In a randomized, double-blind, placebo-controlled, investigator-initiated clinical trial (phase II), 10 patients with SSc and RP-related DUs were randomly and evenly assigned to a placebo control group or treatment group taking BTX-B injections. The degree of improvement in DU, change in size, number of new DUs, improvement in symptoms of RP, and adverse events were recorded.

Enrollment: 10 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. Patients diagnosed with SSc in diagnostic criteria (Appendix 1) by the American-European Rheumatology Association

2. Patients who have Raynaud's phenomenon from consultation, inquiries, etc. judged by Clinical responsibility (sharing) doctor

3. Patients with digital ulcer at acquiring consent The criteria for digital ulcers are as follows.

   • It is a peripheral ulcer from the proximal interphalangeal joint and the thumb interphalangeal joint (including the interphalangeal joint).
   • The continuity of coating by the epithelium has been lost and there is a depth that is visible to the eye. Incidentally, when exposed, cases covered with eschar or necrotic tissue are also included.
   • If the exposure is not clearly recognized (crusted or covered with necrotic tissue), the investigational responsibility (shared) doctor can judge that the epidermis and the dermis are missing.
   • It should not be the paronychia、crack、digital pitting scars.
   • It should not be attached to the projection of the calcification.
   • Size: The maximum diameter (major axis) is 0.5 cm or more.
   • Bones, tendons and joints are not exposed.
   • It is not accompanied by obvious infection findings.

4. At the time of acquiring consent Patients over 18 years old

5. Patients for whom consent has been obtained in writing on participation of this trial

Exclusion criteria

1. Patients with Raynaud's phenomenon due to diseases other than SSc

2. Patients with systemic neuromuscular junction disorder (myasthenia gravis, Lambert-Eaton syndrome, amyotrophic lateral sclerosis etc.)

3. Patients with advanced respiratory dysfunction

4. Patients with a history of hypersensitivity to components of botulinum toxin type B (botulinum toxin type B, human serum albumin, succinate buffer) or other botulinum toxin

5. Patients who received botulinum toxin formulation within 4 months before study drug administration or who have continued efficacy of botulinum toxin at the time of administration of investigational drug even when administered more than 4 months ago

6. Patients who received endothelin receptor antagonist within 60 days before study drug administration

7. Patients who received the following medications within 14 days prior to study drug administration

   • Argatroban hydrate injection
   • Prostaglandin E1 Injection (eg alprostadil injection)

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Quadruple Blind

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10 participants in 2 patient groups

Botulinum toxin group

Experimental group

Description:

400 units in one injection site（0.2mL） Total 2000 units（1.0mL） （For both hands total 4000 units; 2.0 mL）

Treatment:

Drug: Botulinum toxin type B (2500 units / vial)

Physiological saline (control drug) group

Sham Comparator group

Description:

0.2mL in one injection site Total 1.0mL (For both hands total 2.0 mL)

Treatment:

Drug: Physiological saline