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Drug or intervention

Botulinum toxin type A Clinical Trials

Studies that test Botulinum toxin type A, alone, with other treatments or as the comparison.

1,323 registered studies

In numbers

Open to volunteers
150
Active
179
With results posted
350
All registered
1,323

Open to volunteers: recruiting, not yet recruiting or enrolling by invitation. Active adds studies under way that have stopped recruiting.

Open to volunteers

All 150
  • Spinal Cord Injury, Spasticity

    Extracorporeal Shockwave Therapy as an Additional Treatment for Spasticity Secondary to Spinal Cord Injury

    • Recruiting
    • Age: 18 years and older
    • Phase 2
    • Medical device

    Spasticity is a common consequence of spinal cord injury and can have a profound impact on quality of life. The goal of this study is to learn if an intervention called focused extracorporeal shockwave therapy can enhance the…

    Trial name
    NCT07894991
    Testing
    Focused extracorporeal shockwave therapy, Botulinum toxin
    Where
    United States
    Volunteers
    30 people
    Sponsor
    Kessler Foundation
    Can I take part? NCT07894991
  • Hernia Abdominal Wall, Botox Injection

    Preoperative BOTOX® Injection for Large Ventral Hernia Repair

    • Recruiting
    • Age: 18 years and older
    • Phase 4
    • Injection or infusion
    • Surgery or procedure

    This study is for adults who need open surgery to repair a very large abdominal (ventral) hernia. This study tests whether a one-time, image-guided injection of a medicine commonly known as "BOTOX®" (onabotulinumtoxinA) into the…

    Conditions
    Hernia Abdominal Wall, Botox Injection, Hernia Incisional Ventral, Hernia Repair With Compartment Syndrome
    Trial name
    PRETOX (NCT07220382)
    Testing
    OnabotulinumtoxinA Injection, OnabotulinumtoxinA, 0.9 % Normal Saline
    Where
    United States
    Volunteers
    188 people
    Sponsor
    The Cleveland Clinic
    Can I take part? PRETOX
  • Piriformis Muscle Syndrome

    Efficacy of Botulinum Toxin Versus Placebo on Pain and Health Related Quality of Life of Patients With Piriformis Muscle Syndrome

    • Not yet recruiting
    • Age: 18 to 80 years
    • Phase 2
    • Injection or infusion

    Piriformis muscle syndrome (PMS) is characterized by symptoms caused by compression or irritation of the sciatic nerve by the piriformis muscle as it exits the sciatic notch.

    Trial name
    PiriTox (NCT07624045)
    Testing
    Botulinum Toxin - A injections
    Where
    7 sites in France
    Volunteers
    108 people
    Sponsor
    Centre Hospitalier Universitaire de Nīmes
    Can I take part? PiriTox
  • Diabetic Peripheral Neuropathy, Painful Diabetic Neuropathy

    Perineural Botulinum Toxin Injection Versus Oral Duloxetine in Relief of Foot Pain in Painful Peripheral Diabetic Neuropathy

    • Not yet recruiting
    • Age: 30 to 70 years
    • Phase 2

    Painful diabetic peripheral neuropathy (DPN) is a frequent and disabling complication of diabetes that commonly causes persistent foot pain, sleep impairment, and decreased quality of life.

    Conditions
    Diabetic Peripheral Neuropathy, Painful Diabetic Neuropathy, Diabetic Foot Pain, Neuralgia
    Trial name
    NCT07882238
    Testing
    Botulinum Toxin Type A, Duloxetine
    Volunteers
    56 people
    Sponsor
    Assiut University
    Can I take part? NCT07882238
  • Overactive Bladder, Bladder Pain Syndrome

    Migraine Medication Effects on Urinary Symptoms

    • Enrolling by invitation
    • Age: 18 years and older
    • Observational study

    A prospective observational cohort trial to study the effects of CGRP inhibitors (CGRPi) on lower urinary tract symptoms (LUTS) and bladder/pelvic pain.

    Conditions
    Overactive Bladder, Bladder Pain Syndrome, Migraine Disorders, Overactive Bladder Syndrome
    Trial name
    NCT06212661
    Testing
    Ubrogepant, Rimegepant, Atogepant
    Where
    United States
    Volunteers
    200 people
    Sponsor
    The Cleveland Clinic
    Can I take part? NCT06212661
  • Cleft Lip, Cleft Lip Scar

    Cleft Lip Scarring After Botox

    • Recruiting
    • Age: 0 days to 12 months
    • Phase 2
    • Injection or infusion

    This study is investigating whether botulinum toxin type A (Botox) can improve scar appearance after cleft lip repair surgery. Cleft lip repair is commonly performed during infancy, but visible scarring can occur as the incision…

    Trial name
    CLSAB (NCT07880860)
    Testing
    Botulinum Toxin Type A (BOTOX) Injection, Normal Saline
    Where
    United States
    Volunteers
    40 people
    Sponsor
    Children's National Research Institute
    Can I take part? CLSAB
  • Masticatory Myofascial Pain Syndrome

    MRI Study of OnabotulinumtoxinA (OnabotA) Effect on Jaw Muscle Pain

    • Not yet recruiting
    • Age: 18 years and older
    • Phase 2

    The goal of this clinical trial is to learn which magnetic resonance images are best able to assess and predict if a participant with masticatory myofascial pain syndrome will benefit from Botox injections, as compared to placebo…

    Trial name
    NCT07878780
    Testing
    Onabotulinumtoxin A
    Where
    United States
    Volunteers
    120 people
    Sponsor
    Weill Medical College of Cornell University
    Can I take part? NCT07878780
  • Magnesium, Botulinum Toxin Type A

    Can Adjunctive Oral Magnesium Supplementation Prolong the Effect of Botulinum Toxin Type A in Excessive Gingival Display?

    • Enrolling by invitation
    • Age: 18 years and older
    • Pill or oral medicine
    • Injection or infusion

    To evaluate and compare the effect of adjuvant oral magnesium supplementation combined with Botulinum Toxin Type A versus Botulinum Toxin Type A alone on the reduction of millimeter gingival display and the duration of clinical…

    Conditions
    Magnesium, Botulinum Toxin Type A, Excessive Gingival Display, Oral
    Trial name
    NCT07874009
    Testing
    Oral Magnesium Glycinate capsules, ● BoNT-A Injection Alone (Day 0)
    Where
    Egypt
    Volunteers
    26 people
    Sponsor
    Cairo University
    Can I take part? NCT07874009
  • Excessive Gingival Display

    Decision Regret Following Yonsei-Point Botulinum Toxin for Gummy Smile

    • Not yet recruiting
    • Age: 18 years and older
    • Observational study
    • Injection or infusion

    This study evaluates patient-reported decision regret in adult patients who previously received standardized Botulinum Toxin Type A (BoNT-A) injection at the Yonsei Point for excessive gingival display (gummy smile).

    Trial name
    NCT07874022
    Testing
    Botulinum Toxin Type A injection at Yonsei Point
    Where
    2 sites in Egypt
    Volunteers
    32 people
    Sponsor
    Cairo University
    Can I take part? NCT07874022
  • Upper Facial Lines, Glabellar Lines

    A Study to Assess the Safety and Efficacy of Co-Reconstituted TrenibotulinumtoxinE and OnabotulinumtoxinA in Adult Participants With Moderate to Severe Upper Facial Lines

    • Recruiting
    • Age: 18 years and older
    • Phase 2

    The objective of this Phase 2 study is to assess the safety and efficacy of single treatment of trenibotulinumtoxinE and onabotulibumtoxinA combination in adult participants with moderate to severe upper facial lines.

    Trial name
    NCT07871513
    Testing
    TrenibotulinumtoxinE and OnabotulinumtoxinA, OnabotulinumtoxinA
    Where
    United States
    Volunteers
    300 people
    Sponsor
    AbbVie
    Can I take part? NCT07871513

Completed, with results posted

All 298

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