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NCT ID: NCT03713385 Recruiting - Clinical trials for Prediction of Pediatric Endotracheal Tube Size

Comparison Between the Subglotic Diameter and the Epiphyseal Diameter of the Radius in Children for Prediction of Appropriate Endotracheal Tube Sizes

Start date: October 1, 2018
Phase:
Study type: Observational

Background: In pediatric anesthesia, selection of the appropriate endotracheal tube (ETT) size is an important task because the inappropriate one may lead to much complication. The aim of this study is to compare between the subglotic diameter and the epiphysis diameter of radius measured by ultrasonography for prediction of optimum endotracheal tube size in children. Methods: Patients aged from 1 to 6 years will be scheduled for elective surgery under general anesthesia and intubation, were enrolled in this study. Patients were randomly divided into three groups according to method of choosing the tube size. Aged group (n =49): determined the optimal endotracheal tube size according to age of the child (internal diameter [ID] in mm = [age in years + 16] /4) suggested by Cole.4 Subglottic diameter group (n =49): The subglottic transverse diameter was estimated with ultrasonography on the middle of the anterior region of the neck at the level of cricoid cartilage. Epiphyseal diameter group (n =49): the epiphyseal transverse diameter of the distal radius was estimated with ultrasonography. Patient descriptive data, size of the selected ETT, number and size of the optimum tube, number of re-intubation due to incorrect size of ETT either smaller or larger were recorded. Subglottic transverse diameter (mm) and time of intubation were measured. After intubation, pulse, respiratory rate, arterial blood saturation, capnograghy and airway pressure were recorded during surgery. Any airway complications after extubation as edema, stenosis or stridor were also recorded.

NCT ID: NCT03712111 Recruiting - Clinical trials for Cesarean Section Complications

Comparison of Vasopressor Boluses for Management of Hypotension After Spinal Anesthesia

Start date: November 21, 2018
Phase: Phase 4
Study type: Interventional

In this study the investigators will compare the efficacy and side effects of two doses of norepinephrine bolus (6 mcg and 10 mcg) in management of maternal hypotensive episode after subarachnoid block during Cesarean delivery.

NCT ID: NCT03701386 Recruiting - Clinical trials for Cesarean Section Complications

Comparison of N&H Sandwich Technique and Cesarean Hysterectomy in Management of Placenta Accreta Spectrum

Start date: November 1, 2018
Phase: N/A
Study type: Interventional

The placenta accreta spectrum (PAS)is one of the most common reasons for cesarean hysterectomy Which associated with high rates of severe maternal morbidity (40%-50%), with reported mortality rates up to 7%. And, a cesarean hysterectomy might not be considered first-line treatment for women who have a strong desire for future fertility. Conservative management of PAS defines all procedures that aim to avoid peripartum hysterectomy and its related morbidity and consequences. The main types of conservative management which have been described in the literature: the extirpative technique (manual removal of the placenta); leaving the placenta in situ or the expectant approach; one-step conservative surgery and the Triple-P procedure. These methods have been used alone or in combination and in many cases with additional procedures such as those proposed by interventional radiology.

NCT ID: NCT03701191 Recruiting - Gingival Recession Clinical Trials

Using Inverted Periosteal Pedicle Flap in Treatment of Gingival Recession

IPPF
Start date: January 25, 2020
Phase: N/A
Study type: Interventional

Perioteum in the recession defect site will be used as an autogenous graft after raising a flap and the results will be compared with another group which will be treated by the gold standard ( coronally advanced flap with subepithelial connective tissue graft).

NCT ID: NCT03701152 Recruiting - Clinical trials for Negative Pressure Therapy

Comparison Between Two Different Protocols of Negative Pressure Therapy for Healing of Chronic Ulcers

Start date: January 1, 2018
Phase: N/A
Study type: Interventional

Negative Pressure Wound Therapy (NPWT), is a non invasive wound management tool which develops from negative pressure being applied to the wound. This promotes healing through the removal of infectious materials and enhancing granulation tissue formation. NPWT eases debridement as well as promoting healing of different types of wounds.

NCT ID: NCT03701087 Recruiting - Clinical trials for Vitamin D Intake in First Trimester and Incidence of Gestational Diabetes Recurrence

Effect of Vitamin D Intake in Pregnancy to Prevent Recurrence of Gestational Diabetes

Start date: August 2, 2018
Phase: Early Phase 1
Study type: Interventional

primary outcome is vitamin D intake in first trimester for pregnant women with history of gestational diabetes in previous pregnancies and incidence of gestational diabetes recurrence secondary outcome is effect of vitamin D intake on mode of delivery, apgar score and neonatal birth weight

NCT ID: NCT03698734 Recruiting - Missed Abortion Clinical Trials

Evening Primrose Oil Efficacy in Second Trimester Abortion

Start date: November 1, 2018
Phase: Phase 3
Study type: Interventional

efficacy of evening primrose oil in shortening the duration of induction in 2nd trimesteric missed abortion

NCT ID: NCT03698292 Recruiting - Clinical trials for Critically-ill Patients

Itopride in Feeding Intolerance of Critically-ill Patients Receiving Enteral Nutrition

Start date: October 2018
Phase: N/A
Study type: Interventional

The current study will compare the effectiveness as well as the safety of Itopride against metoclopramide as the first line treatment for feeding intolerance in critically ill patients.

NCT ID: NCT03694639 Recruiting - Pain, Phantom Clinical Trials

CT-guided Ganglion Impar Block for Management of Phantom Rectal Pain Syndrome

Start date: June 12, 2018
Phase: Phase 4
Study type: Interventional

Background:Patients underwent abdominoperineal resection with colostomy may suffered from phantom rectum pain syndrome in the perineal area.In this study, the investigators evaluate the combination between ganglion impar block to pregabaline in the treatment of phantom rectal pain syndrome. Method: Forty patients were randomly allocated into 2 groups: Group A (n=20) where patients received pregabaline 150 mg twice daily. Group B (n=20) where patients received pregabaline 150 mg twice daily plus ganglion impar block using 5 ml bupivacaine 5% with 14 mg/2 ml betamethasone.

NCT ID: NCT03687905 Recruiting - Clinical trials for Proliferative Nephritis

Proliferative Lupus Nephritis Treatment With Chloroquine and Hydroxychloroquine

Start date: September 18, 2018
Phase:
Study type: Observational [Patient Registry]

Evaluation the efficacy of chloroquine and hydroxychloroquine in the treatment of proliferative lupus nephritis class III and IV in children and adolescents and evaluate the side effects of both drugs .