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NCT ID: NCT02678936 Withdrawn - Rectal Fistula Clinical Trials

Anal Fistula Repair With Platelet-rich Plasma

Aurora
Start date: November 2015
Phase: Phase 4
Study type: Interventional

Anal fistula is a very common disease with a high impact on life quality. The only commonly accepted treatment option is surgery. A wide range of operations and techniques have been developed all suffering from a relatively high recurrence rate. The investigators propose the combination of the mucosal advancement flap with application of platelet-rich plasma (PRP) in the fistulectomy site. This study aims to test the hypothesis that by applying PRP the healing rate of complicated anal fistulas can be improved in comparison to a control group where the operation is performed without addition of PRP.

NCT ID: NCT02634398 Withdrawn - Clinical trials for Failed Back Surgery Syndrome

A Post Market Study on DRG Stimulation in FBSS (SYMPATHY)

Start date: December 2015
Phase:
Study type: Observational

The purpose of this Post Market Observational Study is to monitor the effect of the Axium® SCS System in the management of chronic pain following surgical lumbar discectomy in subjects whom are routinely scheduled for treatment with the Axium® SCS System.

NCT ID: NCT02562417 Withdrawn - Clinical trials for Neuromuscular Blockade

Impact of iv Dexamethasone on Reversal of Rocuronium-induced Neuromuscular Block by Sugammadex

Start date: June 2016
Phase: Phase 4
Study type: Interventional

Sugammadex is used as a reversal drug for rocuronium- or vecuronium-induced neuromuscular block during general anaesthesia. IV dexamethasone is injected as a prophylactic measure against postoperative nausea and vomiting. Recent animal data have shown that dexamethasone may impair the reversal effect of sugammadex. The objective of this randomised controlled trial is to confirm in the clinical practice these preliminary results.

NCT ID: NCT02519868 Withdrawn - Hypertension Clinical Trials

Chemical Block and Electrical Stimulation of the Carotid Body to Treat Refractory Hypertension

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

High blood pressure, also referred to as hypertension, affects about 65 million people in the United States alone. Approximately 25 percent of people with hypertension cannot control their high blood pressure, despite the use of multiple medications. Recently, new evidence has demonstrated that the carotid body (CB) plays a role in essential refractory hypertension, possibly due to a deregulated, enhanced activity of this organ. Animal studies showed that CB de-afferentiation, through carotid sinus nerve denervation, leads to a long-term stable drop in blood pressure in spontaneously hypertensive rats. De-afferentiation may be performed either by injecting local anesthetics or by electrical stimulation. Both techniques are daily used in the operating theater to anesthetize nerves for a wide range of surgical procedures. We hypothesize that blocking CB with local anesthetics will result in a drop of the blood pressure in refractory hypertensive patients. We also want to test the idea that stimulating the CB with an electrical current will mislead the CB and will also result in a drop of the blood pressure.

NCT ID: NCT02501278 Withdrawn - Clinical trials for Uterine Cervical Neoplasms

A Phase II Clinical Trial of Chemo-radiotherapy in Combination With INO-3112 in Patients With Locally Advanced Cervical Cancer

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

The aim of this study is to assess the potential benefit of the addition of immunotherapy with VGX-3100 and INO-9012 (i.e. INO-3112) to concomitant CRT or, to concomitant CRT and continued as adjuvant in patients with locally advanced cervical cancer. Safety run-in: To test the safety of CRT combined with immunotherapy with INO-3112. This safety run-in phase will include the first 3 patients treated in each of the two INO-3112 combination arms who are exposed to at least two immunotherapy doses and evaluate whether the combination does not pose undue immediate risks to the patients further enrolled in the trial. Phase II:To demonstrate sufficient activity in the experimental combination arms to warrant a further phase III conclusive trial based on progression free survival (PFS) at 18 months assessed by RECIST by the local investigator. The efficacy will be assessed within each experimental arm while the standard arm will serve as a reference arm to check the reliability of the results.

NCT ID: NCT02368249 Withdrawn - Kidney Failure Clinical Trials

Does Terlipressin Improve Renal Outcome After Liver Surgery

TIROL
Start date: January 2020
Phase: Phase 2
Study type: Interventional

The investigators aim to address whether terlipressin improves the renal outcome after liver surgery. Therefore the investigators are planning to conduct a double-blinded randomized control trial. The investigators will randomize patients undergoing any kind of liver surgery and being at increased moderate to high risk for post-operative acute renal failure into a control group receiving post- operative a placebo or into a group receiving post-operatively terlipressin in combination with human albumin.

NCT ID: NCT02308436 Withdrawn - Clinical trials for Erosion of Teeth, Unspecified

Prophylactic Effect of a CANDIDA Mouthwash, Containing the Curolox™ Peptide

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

In vitro results showed a protective effect against acids for the mouthwash containing Curolox™ peptide. The goal of this in situ study is to detect the Curolox™ peptide under natural oral conditions on the tooth surface and to proof the in vitro results obtained. So far there are no effect and safety data of the Curolox™ mouthwash under natural oral conditions available.

NCT ID: NCT02241941 Withdrawn - Burn Injury Clinical Trials

Evaluation of Single-dose Pharmacokinetics of Intravenous Daptomycin in Patients With Thermal Injury

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

The purpose of this study is to determine single dose pharmacokinetics of daptomycin consecutively in 10 patients on three different time points after severe burn injury.

NCT ID: NCT02219139 Withdrawn - Tooth Loss Clinical Trials

A Comparative, Randomized, Prospective, Performance Evaluation of Abutments in Single Tooth Gaps

Start date: December 2012
Phase: N/A
Study type: Interventional

Immunologically evaluation of myeloperoxidase level as indicator for inflammatory reactions on modified surface abutments compared to machined surface abutments.

NCT ID: NCT02199457 Withdrawn - Healthy Volunteers Clinical Trials

A Study to Demonstrate the Clinical Accuracy of the Smartphone Vital Signs System (SVSS)

Start date: July 2017
Phase: N/A
Study type: Interventional

A medical device study to assess the clinical accuracy and equivalence to reference devices of the SVSS to satisfy the requirements of the recognised applicable international standards.