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Signs and Symptoms clinical trials

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NCT ID: NCT04417608 Not yet recruiting - Clinical trials for Finding the Minimum Dose to Induce Sympathectomy in Infraclavicular

Looking for Minimum Dose to Induce Sympathectomy in Infraclavicular Brachial Plexus Block

Start date: June 4, 2020
Phase:
Study type: Observational

For patients who undergoing hemodialysis, it is important to have good AV fistula. One third of AV fistula usually fail during early stage. It is helpful to use nerve block to dilate the blood vessels and enhance the prognosis. But 0.2% Ropivacaine usually cause muscle weakness in present studies. The investigators hope to find the lowest concentration to provide sympathectomy without muscle weakness. Because the patients with hemodialysis usually have multiple co-morbidity, thus we choose patients with forearm fracture at the first place. With this result, the investigators can design further study for patients with hemodialysis. The investigators prefer proximal approach because brachial plexus run together in the cosctoclavicular space and show lower incidence of incomplete work.

NCT ID: NCT04100343 Not yet recruiting - Multiple Sclerosis Clinical Trials

Detection of Pattern of Some Unusual Signs and Symptoms of Multiple Sclerosis

Start date: November 1, 2019
Phase:
Study type: Observational [Patient Registry]

Each Multiple Sclerosis patient will be submitted to Cognitive Abilities Screening Instrument (CASI), Expanded Disability Status Scale, Epowrth Sleeping Scale(ESS),Fatigue Severity Scale(FSS), Hamilton Depression Rating Scale, Hamilton Anxiety Rating Scale, Headache Disability Index, specific questionnaire based on International Headache Society (IHS) recommendations

NCT ID: NCT02824692 Not yet recruiting - Clinical trials for Congestive Heart Failure

Preoperative Significant Clinical Findings Using Focused Ultrasound Examination

Start date: July 2016
Phase: N/A
Study type: Observational

The purpose of this study is to determine whether a focused ultrasound examination for the heart, lungs and abdomen, preformed by a trained anesthesiologist, can reveal significant clinical findings in elderly patients before emergent surgery.

NCT ID: NCT02450565 Not yet recruiting - Chronic Pain Clinical Trials

Translation of the Self Completed-Leeds Assessment of Neuropathic Symptoms and Signs Pain Scale

Start date: July 2015
Phase: N/A
Study type: Observational

Neuropathic pain, described as 'pain arising as a direct consequence of a lesion or disease on the somatosensory system', affects up to 3-9.8% of the investigators' population, but is often underdiagnosed and undertreated. As treatment is different for patients with neuropathic pain and nociceptive pain, it is important to screen for neuropathic pain. Commonly employed questionnaire-based diagnostic tools in English speaking countries include the Leeds Assessment of Neuropathic Symptoms and Signs pain scale (LANSS) and Neuropathic pain questionnaire (NPQ). Self-completed LANSS is particularly useful as it is not restricted to clinician's examination and can be applied in large-scale research. S-LANSS has been successfully translated, validated and used successfully in Arabic and Turkish, but it has not been utilised in the Chinese population. As verbal translations of the English questionnaires used at the bedside may be prone to errors in interpretation and requires medical practitioners to interpret the questions. Therefore a translation and validation study is essential.

NCT ID: NCT01227915 Not yet recruiting - Clinical trials for Acute Bacterial Conjunctivitis

Effectiveness Comparison Between the Drugs TOBRACORT® and TOBRADEX® in Reducing the Signs and Symptoms of Acute Bacterial Conjunctivitis

Start date: February 2011
Phase: Phase 3
Study type: Interventional

The primary objective of this study is to evaluate, through clinical parameters, the comparative efficacy between topical Tobracort ® (tobramycin 0.3% dexamethasone + 1% - Chemistry Lab Union) and TOBRADEX ® (tobramycin 0.3% dexamethasone + 1 % - Alcon Lab), using the percentage of improvement (sustained response rate) at the end of treatment.

NCT ID: NCT01227863 Not yet recruiting - Clinical trials for Bacterial Conjunctivitis

Efficacy Maxinom® And Maxitrol® in Reducing The Signs And Symptoms Of Acute Bacterial Conjunctivitis

Start date: February 2011
Phase: Phase 3
Study type: Interventional

The primary objective of this study is to evaluate, through clinical parameters, the effectiveness of your medicine topic Maxinom ® (dexamethasone, neomycin and polymyxin B - Union Chemicals), comparing it to the topical medication Maxitrol ® (dexamethasone, neomycin and polymyxin B - Alcon ) by the percentage of improvement (sustained response rate) at the end of treatment, among the products studied.

NCT ID: NCT01221142 Not yet recruiting - Hypothermia Clinical Trials

Pilot Study of Hypothermia for Intracerebral Hemorrhage in Croatia

Start date: January 2011
Phase: Phase 3
Study type: Interventional

In this pilot study the researchers will investigate efficacy of hypothermia in the early stage of treatment patients with primary intracerebral hemorrhage.