85 studies found for:    Cephalic Disorders
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Rank Status Study
21 Recruiting Does Bladder Training Improve the Efficacy of Nerve Stimulation in Women With Refractory Overactive Bladders
Condition: Overactive Bladder
Interventions: Behavioral: Bladder Training (BT);   Device: Percutaneous Tibial Nerve stimulation
22 Completed Food Rheology and Feeding in Lean and Obese Humans
Conditions: Obesity;   Overweight;   Diabetes
Interventions: Other: food in fluid form;   Other: food in solid form
23 Terminated Does Chewing Gum After Elective Laparoscopic Colectomy Surgery Decrease Ileus?
Condition: Ileus
Intervention: Other: chewing gum
24 Completed Outpatient Foley Cervix Priming
Condition: Outpatient Mechanical Cervix Priming
Intervention: Other: Outpatient Foley cervix priming
25 Terminated Covered Stents to Treat Hemodialysis Access Stenoses in the Cephalic Arch and Central Veins
Condition: Renal Failure
Interventions: Device: GORE VIABAHN® Endoprosthesis with Heparin Bioactive Surface;   Procedure: PTA alone without use of the GORE VIABAHN
26 Recruiting Drug Eluting Balloon Angioplasty for Recurrent Cephalic Arch Stenosis in Dialysis Fistulas
Condition: Dialysis Access Dysfunction
Interventions: Drug: paclitaxel (Cardionovum Legflow drug eluting balloon);   Device: Balloon angioplasty (Bard Dorado)
27 Recruiting A Comparison of mNT-BBAVF and BCAVF in Hemodialysis Patients
Condition: Vascular Fistula
Interventions: Procedure: mNT-BBAVF;   Procedure: BCAVF
28 Suspended Cerebral Perfusion Monitoring With Transpharyngeal Ultrasonography
Condition: Cardiopulmonary Bypass
Interventions: Device: Transpharyngeal ultrasonography;   Device: Duplex sonography
29 Unknown  Influence of Gum Chewing on Postoperative Bowel Activity After Complete Staging Surgery for Gynecological Malignancies
Condition: Postoperative Ileus
Intervention: Drug: gum
30 Unknown  Cephalic Phase in Anorexia Nervosa,Bulimia Nervosa and Obese Binge Eaters
Conditions: Anorexia Nervosa;   Bulimia Nervosa
Intervention: Procedure: chocolate cake
31 Terminated Clinical Efficacy of a Cephalic Mask for Noninvasive Ventilation During Acute Hypercapnic Respiratory Failure
Condition: Acute Hypercapnic Respiratory Failure
Intervention: Device: Interface for noninvasive ventilation
32 Completed PORTAS 2, Comparing Venae Sectio Versus Punction of Vena Subclavia for Insertion of a Totally Implantable Access Port
Condition: Cancer
Interventions: Procedure: Venae sectio;   Procedure: Punction of V. subclavia
33 Withdrawn Ultrasound Guided Diagnostic Lumbar Medial Branch Blocks
Condition: Back Pain
Interventions: Procedure: Lumbar medial branch block;   Procedure: Ultrasound landmarks
34 Recruiting The LIPMAT Study: Liposomal Prednisolone to Improve Hemodialysis Fistula Maturation
Conditions: Renal Dialysis;   Hemodynamics;   Vascular Remodeling;   Neointima
Interventions: Drug: PEG-liposomal prednisolone sodium phosphate;   Drug: Placebo
35 Recruiting Low or High Ligation of the IMA With Apical Lymph Node Dissection in Rectal Cancer Laparoscopic Surgery
Condition: Rectal Cancer
Interventions: Procedure: Low ligation with apical lymph node dissection;   Procedure: High ligation
36 Not yet recruiting Continuous Pre-peritoneal Wound Infiltration Versus Epidural Analgesia in Cancer Surgery
Condition: Abdominal Neoplasms
Interventions: Device: epidural catheter;   Device: preperitoneal catheter
37 Completed Segmental Epidural Anesthesia (SEA) V/S General Anesthesia for PCNL
Conditions: Success Rate Under Segmental Epidural;   Post Operative Pain
Interventions: Procedure: PCNL under General Anesthesia;   Procedure: Segmental Epidural Anesthesia
38 Completed Validation of the Facial and Cephalic Pain Inventory
Condition: Sinusitis
Intervention:
39 Completed The Randomised Epidural Analgesia in Term Delivering Women Trial (TREAT)
Conditions: Analgesia, Epidural;   Instrumental Delivery;   Maternal Outcome;   Neonatal Outcome
Interventions: Drug: Ropivacaine/ Sufentanil according to local hospital protocol;   Other: Care-as usual pain treatment
40 Completed Cephalic Vascular Recording Upon SPG Stimulation
Condition: Chronic Cluster Headache
Intervention:

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Study has passed its completion date and status has not been verified in more than two years.