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Active clinical trials for "Sialorrhea"

Results 31-40 of 44

Application of Botulinum Toxin Type A in Salivary Glands in the Treatment of Drooling in Patients...

SialorrheaCerebral Palsy

The purpose of this study is to evaluate the safety and efficacy of botulinum toxin-A in salivary glands as a treatment for decrease drooling in patients with cerebral palsy and evaluate the long-term effects and tolerance . To assess whether patients with cerebral palsy have hypersalivation comparing with patients without treatment and healthy volunteers and if botulinum toxin may reduce the volume of drooling without altering the swallowing function.

Unknown status8 enrollment criteria

Ipratropium Bromide Spray as Treatment for Sialorrhea in Children

Sialorrhea

Double-blind, clinical trial investigating the effects of ipratropium spray versus placebo spray in children with sialorrhea

Unknown status7 enrollment criteria

Treatment of Drooling With Type A Botulinum Toxin in Children With Cerebral Palsy

Cerebral PalsyDrooling

The purpose of this study is to evaluate the effectiveness of botulinum toxin injection to treat drooling in children with cerebral palsy, and to find the most appropriate dosage, duration of effect and side effects.

Unknown status10 enrollment criteria

Effectiveness of Kinesiotaping and Manipulation Therapies in Drooling Management Among Children...

Drooling

Children suffering from neurological problems may have a common problem of drooling and dysphagia.There is high prevelance of neurological disorders in developing countries including Pakistan.Parents of children with disability are highly stressed and burdenised while taking care of their children.there is a need to overcome the drooling and dysphagia problems with effective interventions.

Unknown status10 enrollment criteria

The Treatment of 2 Chinese Medicines in Clozapine-induced Hypersalivation in Schizophrenia

SchizophreniaClozapine2 more

The goal of this research is hoping to combine traditional Chinese medicine medication and find out how to solve clozapine-induced hypersalivation, also reduce side-effect, medication compliance, improving life quality, improving social-function and reducing neopathy.

Unknown status11 enrollment criteria

Oral Health Literacy Tailored Communication

Periodontal DiseasesDental Plaque4 more

The purpose of this study to investigate attitude, oral health literacy and psychological factors in order to evaluate if these factors are important for oral health in adults. The hypotheses are: Multiple interactive demographic, and social and psychological factors contribute to the level of attitude and oral health literacy. There is an association between the level of oral health literacy and oral health status A structured intervention based on oral health literacy can change the attitude and improve the oral health status. Background knowledge has influence on attitude and oral health literacy Individuals with positive attitude towards dental health and dentist are attentive towards their oral health.

Completed8 enrollment criteria

Validation of the French Version of the Drooling Impact Scale in a Pediatric Cerebral Palsy Population...

Cerebral PalsyDrooling

The aim of this study is to present the French translation of the Drooling Impact Scale (DIS-F) and to explore its validity, reliability and responsiveness to change in a group of children with Cerebral Palsy (CP)

Completed6 enrollment criteria

FazaClo Outcomes in the Control of Schizophrenia (FOCUS) Study Survey

Weight GainSialorrhea

AZUR Pharma has received several reports from practicing psychiatrists prescribing FazaClo showing that FazaClo patients start losing body weight instead of keep gaining it, after being switched from other clozapine products or other atypical antipsychotics treatments. Another important clinical observation reported by doctors is a considerable reduction in hypersalivation when FazaClo administration is compared to other antipsychotic treatments. Based on the findings described above, and on the real need for effective and safer treatments for schizophrenia, AZUR Pharma has decided to design and conduct an observational study in a large number of patients taking FazaClo to prove the received clinical reports from physicians. Better understanding and evaluation of these beneficial findings are necessary to provide physicians information for improved treatment decision.

Completed20 enrollment criteria

Prevalence of Sialorrhea in Patients Treated With Clozapine

SialorrheaClozapine Adverse Reaction1 more

Clozapine is the "gold standard" antipsychotic drug for the treatment of resistant schizophrenia or resistant psychosis. Despite the high rates of good clinical response, the potential side effects can limit its use. Sialorrhea or excessive salivation is a side effect that occurs in 30-80% of people who receive this treatment and it can cause a decrease in self-esteem and feeling of security, greater social isolation and increase stigma. The main objective of this study is to measure the prevalence of sialorrhea in inpatients and outpatients treated with clozapine and its consequences on the quality of life of people who are receiving this treatment. A total of 129 patients over 18 years of age in treatment with clozapine will be recruited from different units of the Institute of Neuropsychiatry and Addictions (INAD) of the Parc de Salut Mar. Sialorrhea will be evaluated by the nursing team with the Nocturnal Hypersalivation Rating Scale (NHRS), the Scale of Frequency and severity of salivation and the scale of impact on the quality of life. Also sociodemographic variables such as age, date of birth, race, date of diagnosis and clinical variables such as diagnosis, dose of clozapine and other treatments prescribed will be collected.

Completed6 enrollment criteria

Efficacy of Intravenous Glyco-P® in Patients Undergoing Procedure That Require Anesthesia Service...

HypersalivationPrevention of Drooling2 more

This observational study was designed to prove clinical efficacy of the well known "glycopyrrolate" which is considered an orphan drug in Thailand. Since the medication has never been officially used in Thai people and this particular brand "Glyco-P" which was made in India has never been officially proven of its efficacy in Thai people. The study was aimed to prove if this Glyco-P can modestly increase patient's heart rate, decrease secretion and safely used in combination with neostigmine for reversal of non-depo muscle relaxant drugs.

Completed7 enrollment criteria
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