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NCT ID: NCT02992132 Terminated - Clinical trials for Agitation and Aggression in Alzheimer's Disease

Study to Examine the Safety and Efficacy of Pimavanserin for the Treatment of Agitation and Aggression in Alzheimer's Disease (SERENE)

Start date: November 2016
Phase: Phase 2
Study type: Interventional

To evaluate the efficacy of pimavanserin compared with placebo in treatment of agitation and aggression after 12 weeks of treatment

NCT ID: NCT02991898 Terminated - Multiple Myeloma Clinical Trials

Adoptive TReg Cell for Suppression of aGVHD After UCB HSCT for Heme Malignancies

Start date: February 16, 2017
Phase: Phase 2
Study type: Interventional

This is a single center pilot study of a non-myeloablative umbilical cord blood transplant for the treatment of a hematological malignancy with a single infusion of T regulatory (Treg) given shortly after UCB transplantation.

NCT ID: NCT02991768 Terminated - Diarrhea Clinical Trials

Budesonide for Mycophenolic Acid-induced Diarrhea in Renal Transplant Recipients

Start date: January 27, 2017
Phase: Phase 2
Study type: Interventional

The purpose of this study is to learn if using a Entocort (budesonide) to treat diarrhea will be effective and safe for kidney transplant patients, allowing them to continue with MPA medication.

NCT ID: NCT02991547 Terminated - Clinical trials for Adenocarcinoma Esophagus

Surveillance of Patients With Adenocarcinoma of the Gastroesophageal Junction or Esophagus

SAGE
Start date: December 2016
Phase:
Study type: Observational

The purpose of this study is to find out more information about patients who have cancer (adenocarcinoma) of the esophagus or gastroesophageal junction (GEJ) who have been treated with chemotherapy and radiation but have not had surgery. The study will follow patients for 5 years to monitor for their cancer and to see how the standard medical care affects the daily life of patients.

NCT ID: NCT02991430 Terminated - Intervention Clinical Trials

A Non-Invasive Neuromodulation Device for Prevention of Episodic Migraine Headache

Start date: June 30, 2017
Phase: N/A
Study type: Interventional

This study will assess the efficacy of a neuromodulation device for the treatment of episodic migraine headache.

NCT ID: NCT02991196 Terminated - Colorectal Neoplasm Clinical Trials

Antibody DS-8273a Administered in Combination With Nivolumab in Subjects With Advanced Colorectal Cancer

Start date: December 1, 2016
Phase: Phase 1
Study type: Interventional

This trial is being performed in two parts: Dose Escalation and Dose Expansion. The primary objective for the Dose Escalation part is to determine the safety and tolerability at different doses of DS-8273a administered in combination with nivolumab and to identify the dose combination for the Dose Expansion cohort in subjects with mismatch repair (MMR)-proficient advanced colorectal cancer. The primary objectives for the Dose Expansion part are: - To further evaluate the safety and tolerability of DS-8273a administered at the selected dose in combination with nivolumab in subjects with MMR-proficient advanced colorectal cancer - To evaluate preliminary anti-tumor activity of DS-8273a plus nivolumab administered at the selected dose in subjects with MMR-proficient advanced colorectal cancer

NCT ID: NCT02990949 Terminated - Infertility Clinical Trials

The Impact of the Timing of Trigger on IVF Success

Start date: November 2016
Phase: N/A
Study type: Interventional

The aim of this study is to examine the length of ovarian stimulation with the timing of trigger in an IVF cycle and its potential to impact patient outcomes.

NCT ID: NCT02990143 Terminated - Glaucoma Clinical Trials

The Effectiveness of Ologen® Collagen Matrix in Preventing Intraocular Pressure (IOP) Spikes After Ahmed Glaucoma Valve Surgery (AGV-FP7)

Start date: January 15, 2014
Phase: Phase 2
Study type: Interventional

The purpose of this study is to investigate whether placing Ologen over the posterior plate of the Ahmed glaucoma drainage device during initial implantation will allow the formation of a thinner capsule, and decrease the incidence and/or the extent of IOP elevation during the postoperative period.

NCT ID: NCT02990078 Terminated - TBI Clinical Trials

Non-invasive Measurement of Cerebrovascular Reactivity After Traumatic Brain Injury

Start date: December 2016
Phase:
Study type: Observational

The investigators will longitudinally measure cerebrovascular reactivity (CVR) by functional near-infrared spectroscopy (fNIRS) in acute (≤3 days from injury), subacute, and chronic phases after TBI as a biomarker of TCVI as compared to healthy controls. CVR will be measured by fNIRS response to hypercapnia. The investigators hypothesize that CVR will be decreased after TBI and that these decreases will correlate with clinical outcomes. Furthermore, the investigators predict that administration of a vasodilatory medication (sildenafil) will augment CVR after TBI.

NCT ID: NCT02989597 Terminated - Pain, Postoperative Clinical Trials

Intraoperative Methadone Administration for Improved Pain Control in Spinal Fusion Patients

MAPS
Start date: July 29, 2017
Phase: Phase 4
Study type: Interventional

Methadone has several advantages over standard narcotic medications, especially when considering use after a typically painful surgery such as lumbar fusion. Methadone is low cost, has a long half-life, has a convenient dosing schedule, has excellent oral bioavailability, and demonstrates slow onset to withdrawal. The literature comparing methadone to more commonly used post-operative narcotics demonstrates that it manages pain better, sustains consistent plasma concentrations, decreases overall narcotic requirement, results in no additional adverse events, and is safe, even in children, across several studies. Since the standard of care is non-methadone narcotic usage to manage the significant pain of complex spinal surgery cases, it is understandable that methadone could be a desirable alternative to promote sustained pain control and early ambulation in these patients. The goal of this study is to compare the effect of a single dose of methadone administered intraoperatively in enrolled spinal fusion patients to their historical controls given fentanyl and morphine, and determine if more sustained pain control during the first few days after surgery provides a better subjective experience for the patient with less pain, which allows them to ambulate and leave the hospital sooner than patients given a standard regimen.