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NCT ID: NCT02534025 Recruiting - Clinical trials for Liver Transplanatation

Remote Ischemic Preconditioning in Liver Transplantation

RIRI
Start date: January 2016
Phase: N/A
Study type: Interventional

Remote (upper arm) ischemic preconditioning in the donor of living donor liver transplanta to ameliorate the effect of reperfusion injury in recipients.

NCT ID: NCT02533830 Recruiting - Gum Chewing Clinical Trials

Gum Chewing And Bowel Motility in Patients Undergoing Cesarean Section. Kasr el Ainy Experience

RCT
Start date: August 2015
Phase: Phase 4
Study type: Interventional

The aim of the present study was to evaluate the effect of chewing gum on the recovery of bowel function after cesarean section in women.

NCT ID: NCT02531477 Recruiting - Anesthesia Clinical Trials

Intra-carotid Anesthetic Agent Delivery

ICAAD
Start date: January 2015
Phase: N/A
Study type: Interventional

Intra-Carotid delivery of propofol.

NCT ID: NCT02526836 Recruiting - Colon Cancer Clinical Trials

Complete Mesocolic Excision With Central Vessel Ligation Compared With Conventional Surgery for Colon Cancer

Start date: September 2014
Phase: Phase 2/Phase 3
Study type: Interventional

The aim of this study is to compare between complete mesocolic excision with central vascular ligation and conventional surgery of colon cancer regarding number of harvested lymph nodes, surgical outcome and complications.

NCT ID: NCT02522130 Recruiting - Clinical trials for IUD Insertion Complication

Different Analgesics Prior to Intrauterine Device (IUD) Insertion: Is There Any Evidence?

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

Different ways of reducing pain during IUD insertion have been explored. So a randomized study will be conducted to test their role

NCT ID: NCT02521584 Recruiting - Liver Transplant Clinical Trials

Ischemia Time and Graft Survival

Start date: January 2015
Phase: N/A
Study type: Observational

Study the effect of ischemia time on patient and graft survival.

NCT ID: NCT02520765 Recruiting - Infertility Clinical Trials

Obesity Index That Better Predict Ovarian Response

Start date: October 2015
Phase: N/A
Study type: Observational

This study is designed to assess the accuracy of Body Mass Index ,Waist Circumference ,Waist Hip Ratio or Waist Height Ratio as a predictor of ovarian response in women undergoing ICSI.

NCT ID: NCT02504749 Recruiting - Clinical trials for G.I.T. Motility After General Versus Spinal Anaesthesia

The Regain of Gastrointestinal Motility After General Anaesthesia Versus Spinal Anaesthesia in Caesarean Section

Start date: July 2015
Phase: Phase 4
Study type: Interventional

This study aims to compare the time to regain intestinal motility after general anesthesia versus spinal anesthesia for cesarean section. A double blinded randomized controlled trial was conducted at the Department of Obstetrics and Gynecology, Kasr El-Aini Teaching Hospital, Faculty of Medicine, Cairo University, Cairo, Egypt, between July 20 and November 20, 2015. In the study hospital, the total number of deliveries in 2012 was 15 167, 6244 (41.2%) of which were by cesarean; in 2013, the total number of deliveries was 16 057, 5200 (32.4%) of which were by cesarean.

NCT ID: NCT02498522 Recruiting - Clinical trials for Polycystic Ovary Syndrome

Effect of Metformin on Early Pregnancy Loss in Pregnant Women With Polycystic Ovarian Syndrome

MIP
Start date: August 2015
Phase: Phase 0
Study type: Interventional

The aim of this work is to study the effect of metformin use for reducing early pregnancy loss in pregnant patients with Polycystic ovary syndrome (PCOS).

NCT ID: NCT02497053 Recruiting - Clinical trials for Malignant Pleural Mesothelioma

Four Versus Six Cycles of Pemetrexed/Platinum for MPM

Start date: June 2015
Phase: Phase 2
Study type: Interventional

The prognosis of mesothelioma is generally poor. The median survival of patients with unresectable malignant mesothelioma ranges approximately between 6-12 months. Survival is poor because there is no curative treatment. Treatment options include surgery, chemotherapy and radiotherapy. Recently multimodality treatment regimens have been reported to prolong survival. Other new therapeutic approaches include immunotherapy, gene therapy, hyperthermic chemoperfusion of the pleura and photodynamic therapy, but the results have not yet been completely validated. Even with the introduction of this new therapeutic protocol, the response does not exceed 41%, with a mean survival of 12 months. The current standard of care for unresectable malignant pleural mesothelioma is pemetrexed/cisplatin. This regimen was compared to cisplatin alone in a study including 448 patients from 19 countries which was the largest trial to date among patients suffering from malignant mesothelioma. Results showed statistically significant increase in overall survival by about 30 % (12.1 months for pemetrexed /cisplatin versus 9.3 months for cisplatin alone. In addition, there was an improvement in lung function (forced vital capacity) in the pemetrexed /cisplatin arm in comparison to the cisplatin arm. Until now, however, there is no consensus on the number of cycles of pemetrexed/cisplatin in malignant mesothelioma and there are no approved predictive markers for response. Pemetrexed/cisplatin regimen is an expensive regimen and associated with considerable toxicity and so we need to rationalize its use in our Egyptian patients. Therefore, the investigators aim in this work to compare 4 cycles versus 6 cycles of pemetrexed/cisplatin in malignant mesothelioma and to identify a predictive marker for response.