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NCT ID: NCT03152812 Enrolling by invitation - Clinical trials for Best Tissue Constituent for Plantar Surface

Functional Outcome of Free Muscle Flaps Versus Free Skin Flaps for Post-traumatic Foot Plantar Surface Reconstruction

Start date: March 1, 2017
Phase: N/A
Study type: Observational [Patient Registry]

the investigators are trying to detect what is the best tissue constituent suitable for reconstruction of large post traumatic sof tissue defects of foot plantar surface

NCT ID: NCT03115892 Enrolling by invitation - Halitosis Clinical Trials

Green Tea With Aloe Vera Mouthwash and Chlorohexidine Mouthwash

RCT
Start date: April 1, 2017
Phase: Phase 1/Phase 2
Study type: Interventional

The Effect of Mouthwash Containing Green Tea With Aloe Vera and Chlorhexidine Mouthwash on Oral Malodour Among a Group of Egyptian Children: Randomized Clinical Trial

NCT ID: NCT03105960 Enrolling by invitation - Gingival Bleeding Clinical Trials

Garlic With Lime Juice and Chlorhexidine Mouthwash

mouthwash
Start date: March 10, 2017
Phase: N/A
Study type: Interventional

the study about herbal mouthwash. it is clinical trial .the investigator will compare between chlorhexidine mouthwash and garlic with lime juice mouthwash.and their effect on gingival bleeding and plaque and salivary bacteria.

NCT ID: NCT03090061 Enrolling by invitation - Clinical trials for Microleakage Around Resin Composite Restorations

Reliability of Light Induced Fluorescence Intraoral Camera Versus Visual-Tactile Method in Assessment of Marginal Integrity of Resin Composite Restorations: Diagnostic Invivo Study

Start date: July 1, 2017
Phase: N/A
Study type: Interventional

This study will be conducted to assess diagnostic predictive values of a light induced fluorescence intraoral camera versus those of the visual-tactile assessment method according to FDI criteria in clinical evaluation the margins of resin composite restorations

NCT ID: NCT03067064 Enrolling by invitation - Clinical trials for Child Development Disorder

Prevelance of Molar Incisor Hypomineralization Among a Group of Egyptian Children

MIH
Start date: February 17, 2017
Phase: N/A
Study type: Observational [Patient Registry]

The purpose of this study is to find out the prevalence of molar incisor hypomineralization among a group of Egyptian children

NCT ID: NCT03054493 Enrolling by invitation - Child Behavior Clinical Trials

Prevalence of NNSH in a Group of Egyptian Children Aged 3-8 Years Old in Giza Governorate: A Cross Sectional Study.

NNSH
Start date: February 10, 2017
Phase: N/A
Study type: Observational

1. Prevalence of non-nutritive sucking habits (NNSH) in a group of Egyptian children aged 3-8 years old in Giza Governorate. 2. Assessment of factors associated with NNSH.

NCT ID: NCT02996123 Enrolling by invitation - Bites, Human Clinical Trials

Biting Force in Heat Cured Acrylic Resin Versus CAD/CAM Maxillary Single Denture Bases

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

measuring difference in biting force between (computer aided design/computer aided manufacturing) maxillary dentures and conventional ones.

NCT ID: NCT02985281 Enrolling by invitation - Clinical trials for Pharmacological Action

Safety and Efficacy of Gratisovir (Sofosbuvir)- Ribavirin Therapy in Pediatric Patients

Start date: December 2016
Phase: Phase 2/Phase 3
Study type: Interventional

Evaluation of Safety and Efficacy of Gratisovir (Sofosbuvir)- Ribavirin Therapy in Egyptian Pediatric Patients With Chronic Hepatitis C Infection aged 10- 18 years old.

NCT ID: NCT02839083 Enrolling by invitation - Clinical trials for Modified Radical Mastectomy

Pecs II Block as Alternative for Paravertebral Block in Modified Radical Mastectomy

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

Breast surgeries are usually associated with significant postoperative pain. Suitability of analgesic technique after breast surgery is always questionable. The aim of this study is to compare US guided Pecs II block versus thoracic paravertebral block performed by US guidance as regards to potential complications and analgesic efficacy of both techniques in the first 24 h after modified radical mastectomy.

NCT ID: NCT02639013 Enrolling by invitation - Clinical trials for Intraabdominal Hypertension

an Educational Program About Abdominal Compartment Syndrome

Ghada
Start date: December 2015
Phase: Phase 3
Study type: Interventional

Early detection of intra-abdominal hypertension is essential to the prevention of abdominal compartment syndrome and requires close surveillance of intra-abdominal hypertension in patients at increased risk. intra-abdominal hypertension measurements are often taken by the bedside nurse, and in some cases, initiation of serial intra-abdominal hypertension monitoring is prompted by critical care nurses.