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Intra-muscular Botulinum Toxin A in Chronic Athletic Pubalgia

Intra-muscular Botulinum Toxin A in Chronic Athletic Pubalgia: a Retrospective Observational Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05430893
Acronym
PUBATOX
Enrollment
20
Registered
2022-06-24
Start date
2017-06-01
Completion date
2021-03-31
Last updated
2025-09-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Athletic Pubalgia

Keywords

Chronic athletic pubalgia, Botulinum toxin, Groin pain, Adductor enthesopathy

Brief summary

Chronic athletic pubalgia is a frequent sport condition in which the effectiveness of medical treatment has not been proven. Intra-muscular injection of botulinum toxin A may have positive effects on pain in some chronic tendinitis. The investigators hypothesized that similar analgesic effect of intra-muscular botulinum toxin A may be observed in individuals with chronic AP. In the present study, the investigators aimed to describe the short-term evolution of pain and of activity limitations and quality of life, after an injection of the adductor longus with botulinum toxin A, in individuals with chronic AP, for whom medical and/or surgical treatments have failed.

Detailed description

The investigators included consecutive individuals with chronic athletic pubalgia for whom medical and/or surgical treatments have failed and who were treated with an intra-muscular injection of botulinum toxin A under ultrasound guidance. Participants were assessed 50 days after injection for pain using a numerical rating scale (NRS) (0, no pain, and 100, maximal pain) and for activity limitations and quality of life using the Copenhagen Hip and Groin Outcome Score (HAGOS) (0, worse outcome, and 100, most favorable outcome). Participants were also asked to self-report adverse events.

Interventions

OTHERBotulinum Toxin A

100 UI IM in the adductor longus

Sponsors

URC-CIC Paris Descartes Necker Cochin
CollaboratorOTHER
Assistance Publique - Hôpitaux de Paris
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* chronic AP * symptom duration ≥ 3 months * consistent clinical and magnetic resonance imaging findings according to the clinician * failure of medical and/or surgical treatments with persistent pain and inability to return to play * treatment with an intra-muscular injection of botulinum toxin A injection

Exclusion criteria

* age under 18 years * ongoing pregnancy or breastfeeding * treatments by anticoagulants * muscular disorder (e.g. polymyositis, myopathy or other neuromuscular conditions) * guardianship or curatorship * individuals who had received botulinum toxin type A treatment for less than one year

Design outcomes

Primary

MeasureTime frameDescription
Numerical rating scale50 daysMean pain

Secondary

MeasureTime frameDescription
HAGOS score50 daysMean HAGOS total score

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026