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NCT ID: NCT02436343 Completed - Cardiac Performance Clinical Trials

Cardiac Performance in Pregnant Obese Women:Are They in Jeopardy?

Start date: June 2015
Phase:
Study type: Observational

The aim of this work is to Assess serial changes in "cardiovascular function" in morbidly obese pregnant females (BMI equal or higher than 30 kg/m2) as compared to normal lean pregnant female controls.

NCT ID: NCT02426775 Completed - Propionic Acidemia Clinical Trials

Carglumic Acid in Methylmalonic Acidemia and Propionic Acidemia

CAMP
Start date: November 2015
Phase: Phase 3
Study type: Interventional

A Phase IIIb (Three b), Randomized Multicentre Comparative Trial to Evaluate the Long Term Effectiveness & Safety of the use of Carglumic Acid (Carbaglu®) in Patients with Propionic Acidemia (PA) or Methylmalonic Acidemia (MMA). Carbaglu® clinical experience in Organic Acidemia (OA) is limited to a non-comparative retrospective collection of data from patients who had received Carbaglu® for 1 to 15 days. There is no current evidence supporting the use of carglumic acid for the chronic management of patients with OA. The investigators are proposing a randomized multicentre prospective clinical trial to evaluate long-term effects of the use of Carbaglu® (50mg/kg/day) combined with standard chronic therapy in patients with PA and MMA compared to standard chronic therapy alone.

NCT ID: NCT02419534 Recruiting - Fissure in Ano Clinical Trials

Pediatrics Anal Fissures Treatment With Polyethylene Glycol

Start date: November 2014
Phase: Phase 4
Study type: Interventional

To evaluate whether effectively treating anal fissure-associated constipation using oral PEG alone can eliminate the inconvenience of add topical agent such as DTZ. As previous studies have shown the topical agent are more effective in treating anal fissure when combined with less effective laxatives

NCT ID: NCT02407262 Recruiting - Asthma Clinical Trials

Potential Benefits of Black Seed Oil Supplementation on Asthma Inflammation and Outcomes

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

In the Arabic and Islamic culture, Black Seed (Nigella sativa) is a well-known food supplement and herbal product. Traditionally, it is used as a food spice and it has wide range of medical claims that originate from different historical backgrounds. Today in the era of Evidence-based medicine, it is hard to accept those traditional medical claims of medicinal plants without valid scientific experiments. Yet, it is important to rational the uses of these herbal product based on clinical evidence. Asthma is a common chronic disorder of the airways, characterized by variable reversible and recurring symptoms related to airflow obstruction, bronchial hyper-responsiveness, and underlying inflammation. In Saudi Arabia, Asthma is considered one of the leading chronic diseases affecting more than 2 million Saudi citizens. The global Asthma Report 2014 considered Asthma as an epidemic disease probably affecting about 334 million people worldwide and becoming a global health priority. This project investigates the use of herbal products to enhance asthma control in Saudi Arabia. In this context, Black Seed is one of the common herbal products used traditionally for asthma in the Saudi region. Black seed is a common unconventional therapy used among 10% of Asthmatic patients in King Abdulaziz Medical city, Riyadh. In fact, there are some pre-clinical evidence and preliminary clinical studies support the usefulness of Black seed in Asthma and its underlying causes

NCT ID: NCT02405663 Completed - Clinical trials for Complications; Cesarean Section

Methods of Placental Delivery and the Amount of Blood Loss During Cesarean Section

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

To compare between the effect of controlled cord traction and manual removal of the placenta on blood loss among women undergoing caesarean sections

NCT ID: NCT02402244 Recruiting - Clinical trials for Malignant Solid Neoplasm

Project: Every Child for Younger Patients With Cancer

Start date: November 3, 2015
Phase:
Study type: Observational

This study gathers health information for the Project: Every Child for younger patients with cancer. Gathering health information over time from younger patients with cancer may help doctors find better methods of treatment and on-going care.

NCT ID: NCT02386748 Completed - Postoperative Care Clinical Trials

Chewing Gums to Stimulate Intestinal Motility After Cesarean Section

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

The study purpose is to evaluate the efficacy and safety of postoperative gum chewing on the recovery of intestinal movement after cesarean section. All women undergoing elective cesarean section in King Faisal military hospital will be candidate for this trial after full explanation of the trial and informed consent to be taken from the women. Exclusion criteria will include emergency cesarean section, multifetal pregnancy, polyhydramnios, medical disorders with pregnancy, abnormal placentation (previa and/or accreta), past history of bowel injury or operation, any complications that will increase operative duration such as uterine artery injury or uterine extension. 450 consented women for being enrolled in this clinical trial and candidates for elective cesarean section will be divided into 3 groups: - Group A, 150 women will receive sugarless gum after their operating room discharge by 2 hours for at least half an hour at two hours interval. - Group B, 150 women will receive the traditional management of starting oral fluids after operating room discharge by 6 hours and hearing intestinal sounds on second day before initiating full regular diet. - Group C, 150 women as control group, they will not receive neither gum nor oral fluids. They will be in intravenous fluid. All demographic data of these women, indication of operation, operation time, type of anesthesia and pathway during hospital stay will be recovered and compared between 3 groups.

NCT ID: NCT02384486 Completed - Clinical trials for Autism Spectrum Disorder (ASD)

Efficacy of Training Programme to Reduce Stress

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

This study aims to reduce stress in mothers of children with autism in Saudi Arabia. The researcher has designed a training programme for mothers whose children are young and just in their early stage at the autism organisations they are attending. The programme will include stress reduction tips, behavioural modification strategies for children with autism, and financial resources available to parents (how they can access government funding). The study will have two parts. Part one involves conducting an experiment by dividing the participants into two groups, one group will receive the training and the other group will wait until the end of the study then they will also receive the same training. Both groups will fill questionnaire at the beginning of the study, then after the first group finishes training, and then again 6 weeks later. Part two of the study will involve interviewing mothers of the first group who attended the training session. They will be interviewed by the researcher asking them about their experience with the training programme and their suggestions for future improvements. Mothers will be given a training manual at the beginning of the training. Training involves attending five sessions, one of which is a face to face session at the autism organisation their children are attending and the other four sessions will be through a Smartphone application called whatsapp which is widely used in Saudi Arabia.

NCT ID: NCT02375971 Completed - Clinical trials for Retinopathy of Prematurity

RAINBOW Study: RAnibizumab Compared With Laser Therapy for the Treatment of INfants BOrn Prematurely With Retinopathy of Prematurity

RAINBOW
Start date: December 30, 2015
Phase: Phase 3
Study type: Interventional

The purpose of this study was to determine if intravitreal ranibizumab is superior to laser ablation therapy in the treatment of retinopathy of prematurity (ROP).

NCT ID: NCT02372487 Recruiting - Clinical trials for Pregnancy Complication

Sildenafil Citrate Therapy for Oligohydramnios

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

The aim of this randomized trial is to detect whether or not the use of Sildenafil citrate therapy will increase the amniotic fluid volume expressed in term of amniotic fluid index measured via ultrasound for fetuses of pregnancies complicated by oligohydramnios, and to compare the outcomes of Sildenafil-treated pregnancies with similar pregnancies that will remain Sildenafil-naïve.