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NCT ID: NCT03393520 Completed - Clinical trials for Agitation in Patients With Dementia of the Alzheimer's Type

Assessment of the Efficacy, Safety, and Tolerability of AVP-786 (Deudextromethorphan Hydrobromide [d6-DM]/Quinidine Sulfate [Q]) for the Treatment of Agitation in Patients With Dementia of the Alzheimer's Type

Start date: October 13, 2017
Phase: Phase 3
Study type: Interventional

This study will be conducted to evaluate the efficacy, safety, and tolerability of AVP-786 compared to placebo, for the treatment of agitation in participants with dementia of the Alzheimer's type.

NCT ID: NCT03392662 Completed - Air Leakage Clinical Trials

Hemopatch Performance Evaluation: A Prospective Observational Registry

Start date: November 29, 2017
Phase:
Study type: Observational [Patient Registry]

To assess the clinical performance and safety of HEMOPATCH Sealing Hemostat in a post-marketing setting in cardiovascular, thoracic, urologic, neurological, and other general surgical procedures.

NCT ID: NCT03391882 Completed - Clinical trials for Motor OFF Episodes Associated With Parkinson's Disease

A Study of an Investigational Drug to See How it Affects the People With Parkinson's Disease Complicated by Motor Fluctuations ("OFF" Episodes) Compared to an Approved Drug Used to Treat People With Parkinson's Disease Complicated by Motor Fluctuations ("OFF" Episodes)

Start date: December 19, 2018
Phase: Phase 3
Study type: Interventional

A study of an investigational drug to see how it affects the people with Parkinson's Disease complicated by motor fluctuations ("OFF" Episodes) compared to an approved drug used to treat people with Parkinson's Disease complicated by motor fluctuations ("OFF" Episodes)

NCT ID: NCT03390595 Completed - Clinical trials for Metastatic Urothelial Cancer

Avelumab Plus Carboplatin-gemcitabine in Urothelial Carcinoma

INDUCOMAIN
Start date: May 17, 2018
Phase: Phase 2
Study type: Interventional

Phase II Multicentre, randomized, open-label study to evaluate the safety and efficacy of avelumab with gemcitabine/carboplatin versus gemcitabine/carboplatin alone in patients with unresectable or metastatic urothelial carcinoma (UC) who have not received prior systemic therapy and who are ineligible to receive cisplatin-based therapy.

NCT ID: NCT03388099 Completed - Clinical trials for antimüllerian Hormone and Gonadotrophin Receptor Polymorphism as Predictors of Ovarian Response

Impact of Gonadotrophin REceptor Polimorphisms on the Relationship Between Serum AMH and Ovarian Response

GREPAMOR
Start date: January 11, 2018
Phase:
Study type: Observational

Aim of study: To compare the relationship between serum AMH and ovarian response for IVF with the GnRH antagonist protocol in patients who are carriers of FSH and/or LH receptor polymorphisms with those that are not.

NCT ID: NCT03387501 Completed - Infertility Clinical Trials

Concentrate of Autologous Rich Plasma in Growth Factors in the Treatment of the Thin Endometrium

APTE
Start date: May 27, 2019
Phase: Phase 2
Study type: Interventional

This study evaluate the percentage of women with thin endometrium who achieve an endometrial thickness equal to or greater than 7 mm after administration of PRGF (plasma rich in growth factors)

NCT ID: NCT03386994 Completed - Clinical trials for Idiopathic Pulmonary Fibrosis

OASIS-IPF (Idiopathic Pulmonary Fibrosis) Study

Start date: November 29, 2017
Phase:
Study type: Observational

Descriptive prospective non-interventional multicenter study based on newly collected data of Idiopathic Pulmonary Fibrosis patients followed-up for one year in secondary care settings (Pulmonology Services)

NCT ID: NCT03386656 Completed - Clinical trials for Osteoarthritis, Knee

Efficacy and Safety of Topical Application of Tranexamic Acid for Saving Blood Losses in Patients Subjected to Prosthetic Knee Surgery

TRA
Start date: November 28, 2017
Phase: Phase 3
Study type: Interventional

To compare the efficacy and safety of topical tranexamic acid versus placebo in patients diagnosed with severe knee osteoarthritis who will undergo prosthetic knee surgery in terms of saving blood loss (estimated blood loss, decreased hemoglobin and Decrease in hematocrit).

NCT ID: NCT03386630 Completed - Clinical trials for Anesthesia; Functional

Effects of Analgesics in Cesarean Section Elective

CES
Start date: March 28, 2018
Phase: Phase 4
Study type: Interventional

Two approved treatments for spinal anesthesia will be compared in women undergoing cesarean section. It is usual to perform cesarean sections using spinal anesthesia with a local anesthetic (bupivacaine) plus some opioid, such as sufentanil or morphine. Both have been shown to decrease postoperative pain, but we try to check if one brings more benefit than the other.

NCT ID: NCT03386422 Completed - Chronic Pain Clinical Trials

Mindfulness Self-Compassion Intervention Versus a Cognitive-Behavioral Intervention to Improve Self-care in Chronic Pain

Start date: February 3, 2017
Phase: N/A
Study type: Interventional

Approximately 10-23% of people suffer from chronic pain in our country. Chronic pain is associated with emotional distress (anxiety and depression), physical and social impairment and reduction of quality of life in patients who suffer from this condition. Self-Compassion is a useful attitude in order to regulate emotions, to be able to accept the experience that one is going through and to improve self-care in general population. Cognitive-behavioral programs (CBT) have already demonstrated that they are effective in order to reduce catastrophizing and passive coping with pain. However, effects of Mindful Self-Compassion interventions (based on mindfulness skills but not only) on chronic pain condition are still unknown. The investigator's principal hypothesis is: MSC program will be, at least, as effective as CBT program in order to improve quality of life, self-compassion, self-care and acceptance capacity; and as effective as CBT to reduce catastrophizing, anxiety and depression in a chronic pain patients sample. Moreover, investigators also hypothesize that MSC program will be, at least, as effective as CBT program in order to maintain the achieved benefits in a 6 months follow-up. Investigators will conduct a Randomized Controlled Trial with two treatment arms in a chronic pain sample of patients of Hospital Universitario La Paz, Madrid. After all recollection of data is done, investigators will conduct statistic analysis in order to accept or refuse our hypothesis.