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NCT ID: NCT01840878 Completed - Clinical trials for Acute Diverticulitis

Validation of Actigraph Measured Sleep During Acute Diverticulitis

Start date: April 2013
Phase: N/A
Study type: Observational

The purpose of this study is to investigate the accuracy of actigraph measured sleep compared to the golden standard (polysomnography) during Acute uncomplicated diverticulitis. Our hypothesis is the actigraph is accurate for sleep-monitoring for this group of patients

NCT ID: NCT01840852 Completed - Clinical trials for Acute Diverticulitis

Sleep and Cytokines During Acute Diverticulitis

Start date: April 2013
Phase: N/A
Study type: Observational

The purpose of this study is to investigate sleep disturbances during Acute uncomplicated diverticulitis by polysomnography. The investigators hypothesis is the inflammation causes REM(rapid eye movement)-sleep reduction and this is correlated with plasma cytokine levels.

NCT ID: NCT01840800 Completed - Pain, Postoperative Clinical Trials

USG Nerve Blocks for ACL Reconstruction

Start date: February 2013
Phase: N/A
Study type: Interventional

Anterior cruciate ligament reconstruction is a routine surgical procedure. Traditional femoral/sciatic block combinations effectively reduce postoperative pain, but results in considerable motor blockade. The investigators aimed to evaluate postoperative pain relief and the degree of motor block with block combinations of femoral nerve (FEM) and obturator [posterior branch] nerve (ONP), versus saphenous nerve (SAPH) and ONP, versus placebo blocks with isotonic saline. All patients received standard patient controlled analgesia with morphine.Randomized, placebo-controlled and double-blinded clinical trial. Following IRB approval, 81 patients were planned to be randomized to one of three USG block combinations: Active FEM+ONP, active SAPH+ONP or no active blocks (sham blocks) Ropivacaine 0.75% was used for all active blocks following induction of general anaesthesia [propofol-remifentanil, laryngeal mask airway]. Primary outcome measure: Localized PACU pain scores (AUC) 0-6 hours postoperatively at rest. Secondary outcome measures: Opioid consumption, opioid related side effects, PACU time, motor abilities of daily living scores [modified Barthel/100 index], perceived ill health [Short form-8] scores and degree of motor blockade [Jensen- Børglum motor test].

NCT ID: NCT01840410 Completed - Clinical trials for Choroidal Neovascularization (CNV)

Assess the Efficacy/Safety of Intravitreal Ranibizumab in People With Vision Loss Due to Choroidal Neovascularization.

Start date: September 2013
Phase: Phase 3
Study type: Interventional

To evaluate the efficacy and safety of 0.5 mg in adult patients with visual impairment due to choridal neovascularization (CNV).

NCT ID: NCT01840098 Completed - Fasting Clinical Trials

Leucine and Beta-hydroxy-beta-methylbutyrate (HMB) as Anabolic Nutrients After 36 Hours of Fasting

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

The purpose of this study is to investigate metabolic effects of 3 different nutritional compounds. Fasting (36 hours) creates a catabolic state that is comparable with the catabolic state seen in acute illness. This study is a randomized, placebo cross-over study investigating 8 healthy men on 4 separated days (at least 3 weeks between trials). - High leucine content drink - Low leucine content drink - Low leucine content drink + HMB - Carbohydrate (isocaloric) The investigators hypothesize that these nutritional supplements may counteract catabolic processes in different ways and degrees.

NCT ID: NCT01838551 Completed - Clinical trials for Endogenous Cushing's Syndrome

Treatment for Endogenous Cushing's Syndrome

SONICS
Start date: August 2014
Phase: Phase 3
Study type: Interventional

The primary objectives of this study are to evaluate the clinical responder rate, defined as the proportion of subjects with normal UFC after 6 months of treatment with COR-003 in the Maintenance Phase without dose increase, and to evaluate the range of effective doses in subjects with various levels of hypercortisolism.

NCT ID: NCT01837394 Completed - Postoperative Pain Clinical Trials

Ultrasound-guided Blocks for Ambulatory Knee Arthroscopy

Start date: August 2012
Phase: Phase 4
Study type: Interventional

In this study, we wish to investigate the effect of ultrasound (US) -guided block of the saphenous nerve (SN) and the posterior branch of the obturator nerve (ONP) on postoperative pain and the use of opioids (morphine-like pain medicine) in the first 24 hours following ambulatory knee arthroscopy. We wish to investigate the analgesic effect of these two blocks compared to placebo (injection of local anesthetic with known pain blocking properties compared with injection of a saline solution), when used as a supplement to conventional oral analgesics. We hypothesize that patients receiving the active treatment may experience less pain during the first 24 hours after their operation than patients receiving the placebo treatment, and possibly require less opioid analgesics, experience less opioid related side effects and have a higher function level in this period than patients receiving the placebo treatment.

NCT ID: NCT01835002 Completed - Clinical trials for Retinitis Pigmentosa

Transcorneal Electrical Stimulation - Multicenter Safety Study

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

The purpose of this study is to expand the safety assessment of repeated applications of an electrical current from a DTL-like electrode in patients with RP.

NCT ID: NCT01834781 Completed - Clinical trials for Multiple Chemical Sensitivity

Pulsed Electromagnetic Fields for Multiple Chemical Sensitivity

Start date: April 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether pulsed electromagnetic fields(PEMF) is effective in the treatment of multiple chemical sensitivity in terms of life impact, symptoms, psychological distress, markers of central sensitization and the immune system, and quality of life.

NCT ID: NCT01832675 Completed - Clinical trials for Application Site Discomfort

Clinical Trial With Bupivacaine Lozenges as Local Anaesthesia Under Upper Gastrointestinal Endoscopy

Start date: March 2012
Phase: Phase 2
Study type: Interventional

In this project the investigators want to compare a new anaesthetic method during upper gastroscopic endoscopy, compared to the traditional used method in a private clinic. The new method is a lozenge containing bupivacaine, and the traditional method is a lidocaine spray.