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NCT ID: NCT03060681 Recruiting - Spine Surgeries Clinical Trials

Thoracolumber Oterfacial Plane Block for Spine Surgery

TLIP
Start date: February 15, 2017
Phase: N/A
Study type: Interventional

The most commonly used technique to anesthetize patients scheduled for thoracic or lumbar spine surgery is general anesthesia. Analgesic techniques vary from the use of neuraxial techniques like epidural, intrathecal, or caudal analgesia, nerve root infiltration to the use of systemic opioids, Paracetamol, non-steroidal anti-inflammatory drugs (NSAID), steroids and gabapentinoids . In 2015, a promising regional analgesia technique was reported, that targets the dorsal, rather than ventral, rami of the thoracolumbar nerves as they pass through the paraspinal musculature, and called this a thoracolumbar interfacial plane block (TLIP).

NCT ID: NCT03059654 Recruiting - Clinical trials for Tracheostomy Techniques

Ultrasound-guided Percutaneous Dilatation Tracheostomy: Does it Have a Role in Obese Patients?

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

To evaluate the usefulness of ultrasound-guided percutaneous dilatation tracheostomy PCT in obese patients.

NCT ID: NCT03057574 Recruiting - Female Infertility Clinical Trials

Gonapure® in Multifollicular Stimulation in Egyptian Women Undergoing IVF/ICSI

GIVF
Start date: February 9, 2017
Phase: Phase 4
Study type: Interventional

This study aims to record Efficacy, Safety and tolerability of Gonapure® prescribed for female subjects with infertility Undergoing IVF/ICSI

NCT ID: NCT03054558 Recruiting - Clinical trials for Patients With Recurrent Unexplained Pregnancy Loss

JZ Thickness as a Predictor of Recurrent Unexplained First Trimesteric Pregnancy Loss.

JZ
Start date: December 2015
Phase:
Study type: Observational

Patients with history of two or more recurrent pregnancy loss (RPL) and no history of living babies who had performed all investigations for recurrent miscarriage (RM) including : laboratory investigation ,trans vaginal ultrasound (TVS) ,autoimmune work up and hystroscopy and all results were free,will be scheduled for three dimensional trans-vaginal ultrasound (3D TVS) in the midluteal phase for measuring the impedance of uterine artery blood flow( by two dimensional Power Doppler TVS).Also by using 3D power Doppler the sub-endometrial blood flow will be assessed. In addition to the thickness of Junctional Zone (JZ) by using coronal view of 3 D TVS. To be compared with patients who had at least one full term living baby through normal vaginal delivery with no history of early pregnancy loss.

NCT ID: NCT03051594 Recruiting - Dental Caries Clinical Trials

Reliability of Fluorescent Camera and Caries Detection Dye Versus the Visual Tactile Method

Start date: February 3, 2017
Phase: N/A
Study type: Interventional

1. Three dentinal carious lesions will be chosen in this study and will be in the same patient. 2. Using local anaesthesia and rubber dam, the operative field will disinfected with 1% hypochlorite, and the dentine lesions should be exposed with a high-speed diamond bur by removing covering enamel. 3. Before the excavation dentine samples are collected for baseline bacteriological assessment . 4. Excavation will be carried out using new slow speed round burs and hand excavators. 5. The excavation end point of one cavity will be determined using visual tactile method. The two other cavities will be inspected with fluorescent camera or caries detector dye (CDD) methods to determine excavation endpoint respectively. 6. After excavation, dentine samples from the three cavities will be collected using a sterile excavator for the bacteriological assessment. - Number of visits & follow up period: all procedures will be done at the same visit and there is no follow up period. Direct benefit of the research to the human volunteer: to determine the excavation endpoint to ensure complete caries removal and prevent it's recurrence in the future. Scientific value and social benefits: to reach the best method to determine the excavation endpoint. Expected risk to the human subjects: the ordinary side effects associated with any restorative treatment and no of the study variable has side effect on the patient and in case of any side effect due to the restorative treatment, the participant will directly contact the operator.

NCT ID: NCT03051503 Recruiting - Clinical trials for Breast Cancer Female

Efficacy of Transdermal Fentanyl Patches in Relief of Acute Postoperative Pain After Mastectomy

Start date: February 2, 2017
Phase: Phase 4
Study type: Interventional

to determine the safety, efficacy and tolerability of transdermal fentanyl in patients undergoing mastectomy, as well as the postoperative consumption of analgesic.

NCT ID: NCT03047499 Recruiting - Clinical trials for Esthetic Outcome of Injection of Botulinum Toxin Type-A in Cleft Lip Repair

Evaluation of the Effect of Botulinum Toxin Type-A Injection Prior to Surgical Correction of Complete Unilateral Cleft Lip Repair by Modified Millard Cheiloplasty

Start date: February 15, 2017
Phase: N/A
Study type: Observational [Patient Registry]

Evaluation of the effect of botulinum toxin type-A injection prior to surgical correction of complete unilateral cleftlip repair by modified millard cheiloplasty

NCT ID: NCT03046238 Recruiting - Clinical trials for Breast Cancer Patients

Efficacy and Safety of Dexmedetomidine Added to Modified Pectoral's Block in Breast Cancer Patients

Start date: February 2, 2017
Phase: Phase 3
Study type: Interventional

To Evaluate the effect of addition of Dexmedetomedine to ultrasound guided modified Pecs block on post operative analgesia & stress response in patient undergoing modified radical mastectomy.

NCT ID: NCT03044756 Recruiting - Clinical trials for Pituitary Downregulation

Omitting GnRH-antagonist Dose on the Day of Ovulation Trigger

Start date: January 1, 2017
Phase: Phase 2/Phase 3
Study type: Interventional

Omitting the GnRH antagonist on the day of the trigger can be cost effective and more convenient to the women. We will study the impact of omitting the antagonist dose in a prospective randomized trial

NCT ID: NCT03044561 Recruiting - IVF Failure Clinical Trials

Sildenafil Citrate of in Vitro Fertilization After Multiple IVF Failures Attributed to Poor Endometrial Development

Start date: January 31, 2017
Phase: Phase 4
Study type: Interventional

The aim of this study is to evaluate the effect of sildenafil citrate on endometrial development in women with history of recurrent implantation failure after IVF