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NCT ID: NCT03107702 Enrolling by invitation - POSTOPERATIVE PAIN Clinical Trials

Melatonin Level and Postoperative Analgesia Consumption in Bariatric Surgery Patients.

Start date: March 29, 2017
Phase: N/A
Study type: Observational

Bariatric surgical procedures are associated with low short-term mortality and may be associated with long-term reductions in all-cause, cardiovascular, and cancer-related mortality. This surgeries are major surgeries include risk of mortality still. Melatonin is a hormone secreted from the pineal gland. Melatonin is an antioxidant, antinociceptive, hypnotic, anticonvulsant, neuroprotective, anxiolytic, sedative and analgesic. Melatonin is neurohormone with the profile of a novel hypnotic-anesthetic agent. The purpose of this study is to investigate the preoperative, perioperative and postoperative melatonin levels in bariatric surgery under general anesthesia and to investigate the relationship between melatonin level and analgesia requirement.

NCT ID: NCT03069508 Enrolling by invitation - Clinical trials for Hepatocellular Carcinoma

Clemizole HCl for Subjects With Hepatocellular Carcinoma

Start date: February 13, 2017
Phase: Phase 2
Study type: Interventional

This study is a phase IIa open label pilot study of up to six months treatment with clemizole hydrochloride (200 mg vs. 300 mg vs. 400 vs. 500 mg mg) given orally TID to subjects with hepatocellular carcinoma that are either awaiting transplantation or have an unresectable lesion.

NCT ID: NCT02991664 Enrolling by invitation - Clinical trials for Dental Caries Class II

Clinical Performance of a Glass-ionomer Restorative System in Extended-sized Cavities

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

The aim of this clinical trial was to compare the clinical performances of a glass ionomer restorative system with a micro hybrid resin based composite in extended sized class II cavities. A total of 100 class 2 lesions were restored with a glass ionomer restorative system (Equia Forte) or a micro hybrid composite (G-aenial Posterior). Restorations were evaluated at baseline and yearly during 6 years according to the modified-USPHS criteria. Data were analyzed with Cohcran's Q and McNemar's tests (p<0.05).

NCT ID: NCT02679547 Enrolling by invitation - Appendicitis Clinical Trials

The Effect of Breastfeeding on the Development of Appendicitis in Adults

Start date: January 2016
Phase:
Study type: Observational

Appendectomy is the most common emergent operative procedure performed worldwide. In this study investigators will investigate if there is a relationship between breast feeding and appendicitis in adults.

NCT ID: NCT02676479 Enrolling by invitation - Clinical trials for Genetic Diseases, Inborn

Uterine Irrigation Method in Infertility Patients Who Require PGD

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

The study will involve up to 30 pairs of male and female sexually intimate partners who are carriers for a genetic disease (e.g Sickle Cell Disease or Thalassemia) and at high risk of transmitting the gene. The female partner will be superovulated to mature multiple oocytes which can be fertilized, inseminated with her partner's sperm through intra-uterine insemination (IUI). Four to six days after IUI, the female partner will undergo a non-surgical uterine lavage procedure to recover preimplantation embryos.

NCT ID: NCT02036411 Enrolling by invitation - Infertility Clinical Trials

Does Clomiphene Citrate Used for Induction of Ovulation Effect Levels of AMH and Inhibin B

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

100mg clomiphene citrate used for ovulation induction. The investigators take blood sample at 3 and 10 days of menstruation and count AMH and inhibin B.

NCT ID: NCT01816269 Enrolling by invitation - Clinical trials for Helicobacter Pylori Infection

Effect of Dental Scaling on Helicobacter Pylori Eradication and Reinfection

Scaling and Hp
Start date: March 2013
Phase: N/A
Study type: Observational

Patients who had received H.pylori eradication treatment will be categorised as eradication and reinfection status and whether dental scaling has any influence on these results.

NCT ID: NCT01804686 Enrolling by invitation - Clinical trials for Chronic Lymphocytic Leukemia

A Long-term Extension Study of PCI-32765 (Ibrutinib)

CAN3001
Start date: September 9, 2013
Phase: Phase 3
Study type: Interventional

The purpose of this study is to collect long-term safety and efficacy data for participants treated with ibrutinib and to provide ongoing access to ibrutinib for participants who are currently enrolled in ibrutinib studies that have been completed according to the parent protocol, are actively receiving treatment with ibrutinib, and who continue to benefit from ibrutinib treatment.

NCT ID: NCT01533571 Enrolling by invitation - Clinical trials for Unspecified Atrophy of Edentulous Alveolar Ridge

Immediate Implant Placement in the Esthetic Zone

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

This study aims to examine dimensional alveolar ridge alterations and prevent buccal plate resorption and soft tissue recession following immediate implant placement in extraction sockets in the maxillary esthetic zone using different socket morphology-guided treatment modalities. Expected results of the study are: - To have found the optimal materials and GBR procedures modalities for buccal plate resorption degree reduction; - Soft tissue recession and best esthetic result achievement. There will be possibilities to study socket morphology influence on final esthetic result achievement.

NCT ID: NCT01172158 Enrolling by invitation - Stents Clinical Trials

SMS Reminder for Forgotten Ureteral Stents

sms&FUS
Start date: May 2010
Phase: N/A
Study type: Observational

Ureteral stents has become an indispensable instrument for urology practice as a result of widespread use of endourological interventions. Removal of stents could be sometimes neglected by patients or physicians. This omission may lead to legal and medical problems for urologists, health institutions and also for patients. In this study, the investigators offer a computer program providing two sided recall to prevent this nasty complication with sending automatic message by short message service (SMS) to both the patient and the urologist.