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Botulinum Toxin Relieves Anxiety, Depression and Sleep Disorderes in Patients With Blepharospasm

Botulinum Toxin Relieves Anxiety, Depression and Sleep Disorderes in Patients With Blepharospasm

Status
UNKNOWN
Phases
Early Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04939909
Enrollment
50
Registered
2021-06-25
Start date
2021-07-12
Completion date
2022-07-15
Last updated
2022-07-19

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

Conditions

Blepharospasm

Brief summary

Blepharospasm (BSP) is a chronic, idiopathic, recurrent and progressive disease, which mostly occurs in both eyes. It is mainly manifested as involuntary spasm of muscles around the eyes, leading to uncontrollable narrowing or even closure of blepharospasm. Although there is no pain in BSP patients, it can cause social or psychological dysfunction, make patients feel difficult in driving, reading and working, and seriously affect the social, work and life of patients. Depression and anxiety are common and harmful mental disorders. At present, less than 40% of patients with depression can get effective treatment. Using simple and effective screening tools can effectively improve the detection rate of depression, so that patients can get timely and effective treatment. It is also an effective measure to prevent suicide. Botulinum toxin type A (BTX-A) has achieved gratifying results in the treatment of dyskinesia. It has been confirmed that BTX-A has a significant effect on BSP. The effective rate is 70% - 90%. About 50% of the patients can regain normal or near normal visual function. At present, no prospective studies have explored this association between blepharospasm and depression / anxiety, and whether BTX-A can improve this mood disorder. Therefore, our research goal is to further study the relationship between blepharospasm and depression / anxiety, sleep in a prospective way, and to determine whether BTX-A treatment will affect depression / anxiety symptoms, so as to provide more theoretical basis for clinical treatment.

Interventions

DRUGBotulinum toxin type A

Patients were treated with Botulinum toxin type A applications on the Orbicularis oculi and glabellar complex

Sponsors

Second Affiliated Hospital, School of Medicine, Zhejiang University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
40 Years to 70 Years
Healthy volunteers
Yes

Inclusion criteria

* Patients with blepharospasm who received botulinum toxin injection therapy * All patients must have had the symptoms of blepharospasm for over six months

Exclusion criteria

* Glaucoma * Age-related macular degeneration * Visual acuity of 20/200 or worse * Chronic obstructive pulmonary disease * Cardio cerebral diseases, psychosis * Loss of limb * Connective tissue diseases * Dialysis dependence * Anyone who was unable to cooperate with the examinations

Design outcomes

Primary

MeasureTime frameDescription
Change from baseline blepharospasm evaluation at 3 monthsThrough study completion, 3 months.Patients will evaluated the Jankovic Rating scale (JRS),the total score of JRS is 8, and a change of 2 points in the JRS is clinically meaningful.

Secondary

MeasureTime frameDescription
Change from baseline depression evaluation at 3 monthsThrough study completion, 3 months.Patients will evaluated the personal Health Questionnaire Depression Scale (PHQ-8) with a total score of 24, cut-points of 5, 10, and 15 represent mild, moderate, and severe levels of depressive symptoms.
Change from baseline anxiety evaluation at 3 monthsThrough study completion, 3 months.Patients will evaluated the Generalized Anxiety Disorder 7-item scale (GAD-7) questionnaires with a total score of 21, cut-points of 5, 10, and 15 represent mild, moderate, and severe levels of anxiety symptoms.

Other

MeasureTime frameDescription
Change from baseline sleep disorders evaluation at 3 monthsThrough study completion, 3 months.Patients will evaluated the Athens insomnia scale (AIS) questionnaires, the severity criteria of the AIS are capable of categorizing insomnia severity as follows: absence of insomnia (0-5), mild insomnia (6-9), moderate insomnia (10-15), and severe insomnia (16-24).

Countries

China

Contacts

Primary ContactJuan Ye
yejuan@zju.edu.cn057187783897
Backup ContactHuina Zhang
zhanghuina@zju.edu.cn0571-87783897

Outcome results

None listed

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