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Spasm clinical trials

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NCT ID: NCT02832115 Completed - Clinical trials for Coronary Artery Disease

Topical Nitroglycerine Treatment for Radial Artery Spasm Prevention

TNT-RASP
Start date: September 2016
Phase: Phase 4
Study type: Interventional

The primary objective of the study is to determine the role of transdermal vasodilators as an adjunct to parenteral vasodilators in reducing radial artery spasm, improving patient comfort, and post procedure radial artery patency during transradial coronary angiograms and interventions. The study hypothesis is that transdermal vasodilators will increase radial artery size and reduce radial artery spasm as well as improve patient comfort and post procedure radial artery patency. This is a single-center, double-blind, randomized, placebo-controlled study comparing the effect of transdermal preparations of lidocaine + nitroglycerine and lidocaine + placebo on radial artery spasm in patients undergoing transdermal coronary angiograms. Prior to the procedure, each patient will be randomized into either the control arm, lidocaine + placebo, or study arm, lidocaine + nitroglycerine.

NCT ID: NCT02829827 Terminated - Clinical trials for Infantile Spasms (IS)

A Phase 2 Study of Radiprodil in Subjects With Drug-resistant Infantile Spasms (IS)

Start date: December 4, 2017
Phase: Phase 2
Study type: Interventional

The purpose of the study is to evaluate the safety and tolerability, the pharmacokinetics and the efficacy of radiprodil in abolishing clinical spasms in subjects with drug-resistant infantile spasms

NCT ID: NCT02814565 Completed - Neck Pain Clinical Trials

Cyclobenzaprine HCl Extended Release 15 mg Versus Placebo in Treatment of Cervical and/or Lower Back Pain Due to Muscle Spasms of Local Origin

Start date: October 12, 2016
Phase: Phase 3
Study type: Interventional

The purpose of this study was to assess the effect of cyclobenzaprine hydrochloride (HCl) extended release (CER) 15 mg capsule once daily in participants with muscle spasms associated with acute painful musculoskeletal conditions.

NCT ID: NCT02642874 Recruiting - Liver Cirrhosis Clinical Trials

Methocarbamol in Treatment of Muscle Cramps in Cirrhotic Patients

Start date: April 1, 2017
Phase: Phase 3
Study type: Interventional

Muscle cramps markedly affect the quality of life in cirrhotic patients with no highly effective drug. Methocarbamol is a central muscle relaxant used to treat skeletal muscle spasms. The mechanism of action of methocarbamol is currently unknown, but may involve the inhibition of carbonic anhydrase. Methocarbamol has a high therapeutic index, i.e. a wide range of safe and effective dosages.

NCT ID: NCT02642861 Not yet recruiting - Liver Cirrhosis Clinical Trials

Cyclobenzaprine in Muscle Cramps With Liver Cirrhosis

Start date: October 2018
Phase: Phase 3
Study type: Interventional

- Cyclobenzaprine, is a muscle relaxer medication used to relieve skeletal muscle spasms. It is one of the best-studied drug for this application.

NCT ID: NCT02642484 Not yet recruiting - Liver Cirrhosis Clinical Trials

Gabapentin in Treatment of Muscle Cramps in Patients With Liver Cirrhosis

Start date: December 2018
Phase: Phase 3
Study type: Interventional

- Muscle cramps markedly affect the quality of life in cirrhotic patients with no highly effective drug. - Quinine was suggested for treatment of patients with muscle cramps in patients with liver cirrhosis. However, thrombocytopenia, cardiac arrhythmias and cinchonism are serious side effects.

NCT ID: NCT02577796 Withdrawn - Arterial Occlusion Clinical Trials

Radial Artery Spasm Leading to Occlusion in Patients Undergoing Coronary Angiogram Via Radial Access

Start date: December 1, 2014
Phase:
Study type: Observational [Patient Registry]

Radial artery access is increasingly becoming popular among interventional cardiologists for patients undergoing percutaneous coronary intervention(PCI)/ diagnostic angiography secondary to its low complications rates. However, it is frequently associated with the spasm of the radial artery which can lead to difficulty in catheter manipulation during the procedure and potentially leading to vessel trauma. This vessel trauma can cause activation of coagulation system and formation of clot and subsequently the occlusion of radial artery. In this study the investigators intend to find the association of radial artery spasm with the future development of radial artery occlusion in patients who undergo PCI via radial access.

NCT ID: NCT02577224 Completed - Blepharospasm Clinical Trials

An RCT of a Patient-initiated Treatment Service for BEB and HFS

Start date: August 2015
Phase: N/A
Study type: Interventional

Blepharospasm and hemifacial spasm are debilitating conditions which significantly impact on patient quality of life. Cyclical treatment with botulinum toxin injections offers temporary relief but the duration of treatment efficacy is variable. The standard model of patient care defines routine fixed- time based scheduled treatment cycles which may lead to unnecessarily frequent treatment for some patients and experience of distressing symptoms in others if symptoms return before the scheduled follow up period. The present study aims to compare a patient-initiated model of care, where patients determine treatment timing, with the standard model of care by using a two-arm randomised controlled trial design. It is expected that patients able to initiate their own treatment will experience less variation in disease severity and disability over a treatment cycle as they will be empowered to take the initiative when they feel they need to have treatment. A range of other outcomes will be assessed including: confidence and satisfaction in the service, depression, anxiety, quality of life and, illness and treatment beliefs. If the patient-led care model is shown to be effective in preventing distress and reducing disability in these populations; and is found to be acceptable to service users, this will have significant implications for service organisation across the NHS.

NCT ID: NCT02561702 Completed - Clinical trials for Charcot Marie Tooth Disease

Mexiletine for Muscle Cramps in Charcot Marie Tooth Disease

Start date: September 2015
Phase: Phase 2
Study type: Interventional

Charcot Marie Tooth Disease is a family of inherited peripheral neuropathies, with over 70 causative genes identified to date.1-4 Muscle cramps are frequent in CMT, affecting up to 85% of patients with some subtypes of CMT. These cramps impact quality of life and have been identified as an important therapeutic target for clinical trials in CMT.1-4 There is no FDA approved treatment for muscle cramps.5 Mexiletine is a sodium channel blocker approved for treatment of arrhythmias. As a sodium channel blocker, mexiletine offers the promise of effective therapy for muscle cramps.

NCT ID: NCT02551731 Terminated - Spasms, Infantile Clinical Trials

Cannabidiol Oral Solution for Treatment of Refractory Infantile Spasms

Start date: January 27, 2016
Phase: Phase 2
Study type: Interventional

Infantile Spasms (IS) is a diagnosis described as a fairly rare and terrible form of epilepsy that usually strikes children in the first year of life. There is a great need for safe and effective therapies in the treatment of IS. This need is even more important for infants and toddlers still sick after being treated with medicine that is already available. This is a multi-center study to evaluate the efficacy and safety of Cannabidiol Oral Solution (CBD) in the treatment of children aged 6 months through 36 months with a diagnosis of infantile spasms who have not responded to first line therapies. The overall study duration is expected to be 64 weeks for those subjects who respond to CBD treatment. The maximum possible study duration for each patient is approximately 64 weeks, however a subject will be deemed to have completed the study after 58 weeks.