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NCT ID: NCT02234466 Enrolling by invitation - Breast Cancer Clinical Trials

Preoperative Oral Dexamethasone to Improve Recovery After Surgery

Start date: August 2014
Phase: Phase 2
Study type: Interventional

Randomized controlled trial of pre-operative oral dexamethasone vs placebo for the improvement of quality of recovery from surgery. The study population is limited to breast surgery patients. The investigators will also look at the effect of our intervention on post operative nausea and vomiting. Patients will be recruited before the date of their surgery and will complete the Quality of Recovery-40 (QOR-40) questionnaire before their surgery and at 24 hours post op. They will also complete a Clinically significant nausea and vomiting score upon discharge from the post anesthesia recovery room, repeated at 24 hours post op.

NCT ID: NCT02257034 Enrolling by invitation - Fibromyalgia Clinical Trials

The Effect of Tai Chi in Treating Fibromyalgia

Start date: August 2014
Phase: N/A
Study type: Interventional

To evaluate the effect of Tai chi on Fibromyalgia

NCT ID: NCT02258269 Enrolling by invitation - Clinical trials for Rheumatoid Arthritis

The Effect of Square Dance on Rheumatoid Arthritis

Start date: August 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to observe the effect of square dance on rheumatoid arthritis.

NCT ID: NCT02264301 Enrolling by invitation - Clinical trials for Rheumatoid Arthritis

Qingkailing Injection Versus Puerarin Injection on Withdrawal Rate of Corticosteroids in Patients With Active Rheumatoid Arthritis

Start date: August 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the effect of Qingkailing injection versus Puerarin injection on withdrawal rate of corticosteroids in patients with active rheumatoid arthritis.

NCT ID: NCT02270723 Enrolling by invitation - Clinical trials for Hemorrhage; Complicating Delivery, Coagulation Defect

The Effect of Human Albumin on Coagulation Competence and Hemorrhage

Start date: August 2014
Phase: Phase 4
Study type: Interventional

In a randomized clinical trial, the purpose is to investigate if perioperative coagulation and hemorrhage is influenced by colloid or crystalloid.

NCT ID: NCT02275247 Enrolling by invitation - Clinical trials for Intracranial Aneurysm

Perioperative Neuroprotection of Stellate Ganglion Block

Start date: August 2014
Phase: N/A
Study type: Interventional

To investigate whether stellate ganglion block is helpful to brain protection during cranial aneurysm surgery

NCT ID: NCT02306421 Enrolling by invitation - Mixed Hemorrhoids Clinical Trials

A Multi Center Clinical Trial of Rph With the Simplified Milligan-Morgan Surgery on Treatment of Mixed Hemorrhoids

RPHSMMH
Start date: August 2014
Phase: N/A
Study type: Interventional

Simplified Milligan-Morgan is a surgical option which was improved and developed by Professor He,well-known traditional Chinese doctor from Hunan province,based on Milligan-Morgan.RPH is a new therapy for hemorrhoid following the improvement of rubber band ligation.RPH +Simplified Milligan-Morgan is one of important means of modern surgery.The operation method was improved and developed on the basis of Chinese medicine traditional loop ligature and it also embodies uniqueness and advantage of the treatment of mixed hemorrhoids combined traditional Chinese and Western Medicine.The study intends to compare five surgery ways through 3000 cases of patients with mixed hemorrhoid from 12 hospitals,observing the efficacy and safety of various operative methods.Exploration of RPH + Simplified Milligan-Morgan operation indication, contraindication, operation steps and key points, and the operation complications and sequelae and treatment etc provide evidence of evidence-based medicine for Clinical application.

NCT ID: NCT02307994 Enrolling by invitation - Oligospermia Clinical Trials

Clinical Research on Effectiveness and Safety of Treatment of Severe Oligospermia or Azoospermia With uFSH

Start date: August 2014
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether uFSH is effective and safe in the treatment of male patients with severe oligospermia or azoospermia.

NCT ID: NCT02342262 Enrolling by invitation - Migraine Clinical Trials

The Effect of Probiotics on the Frequency and Intensity of Migraine Attacks and Intestinal Permeability

Promi2
Start date: August 2014
Phase: N/A
Study type: Interventional

RATIONALE: The prevalence of migraine is higher in patients with various intestinal diseases. An explanation could be that migraine is caused by a 'leaky gut': an increased intestinal permeability that allows food particles to pass the gastrointestinal wall. Probiotics may be able to improve intestinal barrier function. OBJECTIVE: To test whether probiotics, as adjuvant therapy, can reduce incidence and severity of migraine attacks by reducing intestinal permeability. STUDY DESIGN: 12-week placebo-controlled randomized double-blind intervention with selected probiotics. STUDY POPULATION: Adults who experience at least 4 migraine attacks per month. INTERVENTION: Subjects will receive either one daily dose of 2 g of Ecologic® Barrier or 2 grams of the placebo, containing only the carrier material (both provided by Winclove Probiotics). MAIN STUDY PARAMETERS/ENDPOINTS: Incidence and severity of migraine attacks, measured by diaries and validated headache questionnaires will be measured at baseline and after 4, 8, and 12 weeks of probiotic/placebo administration. Secondary, intestinal permeability will be measured by the lactulose/mannitol absorption test in urine (screening, baseline and 12 weeks) and by fecal zonulin (baseline, 4, 8, and 12 weeks). Inflammation will be assessed from blood C-reactive protein and cytokine concentrations (baseline, 4, 8, and 12 weeks). Fecal samples will also be used for microbial analysis.

NCT ID: NCT02368938 Enrolling by invitation - Clinical trials for Cardiovascular Risk Factor

Prognosis in the Elderly Chinese: the Northern Shanghai Study

NSS
Start date: August 2014
Phase: N/A
Study type: Observational

The Northern Shanghai Study is a prospective community-based study, which is aimed to investigate the prognostic factors, including conventional cardiovascular risk factors and asymptomatic target organ damage, for mortality and cardiovascular diseases, in 5,000 elderly Chinese.