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NCT ID: NCT04975503 Completed - Clinical trials for Cardiovascular Diseases

Risk Factors in Young Middle Eastern Women With Cardiovascular Disease

Start date: August 22, 2021
Phase:
Study type: Observational

Cardiovascular disease continues to be the leading cause of death among women in the Middle East, including Jordan. Sex-specific data focused on cardiovascular disease have been increasing steadily, yet is not the subgroup of young women. This study focuses on classical and novel risk factors of cardiovascular disease in young women compared with older women.

NCT ID: NCT04967586 Completed - Covid19 Clinical Trials

Medical Students and Risk of COVID-19 Infection

Covid 19
Start date: December 1, 2020
Phase:
Study type: Observational

This study aims to estimate the prevalence of infected medical students with COVID-19 in the University of Jordan and to compare number of cases between students in clinical and basic years. In addition, this can provide insight into the awareness of infection control practices among students. Furthermore, to examine if hospital rotations increased risk of infection between clinical year medical students.

NCT ID: NCT04944212 Completed - Clinical trials for Vitamin D Deficiency

Prevalence of Vitamin D Deficiency in Pregnant Women and Their Fetus in North Jordan

Start date: October 31, 2021
Phase:
Study type: Observational

In Jordan, there are few data about the prevalence of hypovitaminosis D in pregnant women and their newborns and factors that affect their levels. Hence, in this study, investigators will : 1. Determine vitamin D levels among newborns born in north Jordan 2. Determine vitamin D levels among pregnant women in north Jordan 3. Study the association between maternal and infants levels of vitamin D 4. Explore the association between maternal and fetal characteristics and maternal and/or fetal vitamin D level 5. Study the effect of low fetal vitamin D on newborn anthropometry 6. Study the effect of maternal vitamin D supplement use during pregnancy in raising cord serum vitamin D levels

NCT ID: NCT04941820 Completed - Surgical Patients Clinical Trials

The Impact of Clinical Pharmacist in the Identification and Management of Treatment Related Problems in the Surgery Ward

Start date: September 29, 2019
Phase: N/A
Study type: Interventional

Patients in the surgery ward are at risk of morbidity and mortality from various types of treatment-related problems (TRPs). The primary aim of this study is to assess the impact of the clinical pharmacist in the identification and management of TRPs in the surgery ward.

NCT ID: NCT04936373 Completed - Health, Subjective Clinical Trials

Quality of Life of Patients With Pregnancy Related VTE

Start date: October 1, 2020
Phase:
Study type: Observational

A retrospective study of the quality of life and problems experienced by patients who developed pregnancy related VTE. It involves patients seen at JUH in 2012-2020. A questionnaire will be filled by those patients and any other patients in Jordan. It was translated to an Arabic form from EQ-5D, VEINES-QOL/SYM questionnaire and PEmb-QoL. The quality of their lives will be assessed and the problems encountered are going to be analyzed to try to find some solutions. This project is going to be a national research project with the efforts to try to find common platforms for those patients and nidus to establish a national support group.

NCT ID: NCT04932733 Completed - Healthy Clinical Trials

Isometric Exercises in Healthy Elderly Individuals

Start date: February 15, 2021
Phase: N/A
Study type: Interventional

A total of 58 participants were selected and divided into two groups equally, namely, elderly, and young groups with the age groups of 60-80 years and 20-30 years, respectively. The Heart Rate (HR), Respiratory Rate (RR), Blood Pressure (BP), Oxygen Saturation (SaO2), and Mean Arterial Pressure (MAP) for each participant were assessed before and after the treatment session.

NCT ID: NCT04870242 Completed - Appendicitis Clinical Trials

Studding the Implementation of ERAS Protocols in Pediatric Surgery

Start date: May 1, 2020
Phase:
Study type: Observational

this is a retrospective cohort, descriptive study, investigating the role of ERAS protocols, in pediatric surgery and evaluate the feasibility and effectiveness of implementing these protocols

NCT ID: NCT04869202 Completed - Perinatology Clinical Trials

Covid-19 Infection in Pregnancy

Start date: December 1, 2020
Phase:
Study type: Observational

Prospective study of both maternal and fetal outcomes of those pregnancies that were complicated by COVID-19 infection at various gestational ages. The follow up will be from the time the diagnosis was made till discharge of the mother and her baby from the hospital.

NCT ID: NCT04824586 Completed - Diabetes Mellitus Clinical Trials

Intraoperative Insulin Administration at Cardiac Surgery for Diabetic Patients

Start date: June 1, 2019
Phase: Phase 4
Study type: Interventional

The primary objective of the study was to explore which insulin-based regimen is better, infusion or bolus regimen, for intraoperative management of glucose level for the diabetic patient at cardiac surgery. Secondary objectives include: comparing the relative amounts of insulin needed during the operation and subsequent cost impact and comparing potassium levels between groups. Ethical approval for the study was obtained from the Office for Research Ethics Committees at Hashemite University - Prince Hamza hospital. This study was a parallel-group, randomized, controlled trial with 1:1 allocation ratio. Participants: Adult diabetic patients, type 2, who were admitted to hospital for cardiac surgery. The intervention: Both patients in the infusion or bolus group received their dose of insulin, fast-acting human insulin (Actrapid®) was used. Setting: Patients were recruited at Prince Hamza hospital, Amman, Jordan. A tertiary care center specialized unit in cardiac surgery for diabetic patients. Outcomes monitoring: It was monitored six times as follows: preoperative induction measure, then glucose post heparin, and after that for 2 hours, glucose levels were monitored every 30 minutes. Insulin quantities were recorded as well to be used in secondary outcomes analysis. Randomization, allocation, and blinding During patient enrolment, concealed allocation to either infusion group or bolus group was guaranteed through the use of a closed envelope system prepared by an independent investigator. Block randomization with random block sizes, ensured allocation balance, and avoided selection bias by preventing allocation prediction. Researchers and physicians were blind to the block size sequence and randomization. Envelopes were unopened until completion of patient registration. Hospital staff who monitor glucose and those who administered insulin were blinded to the primary and secondary outcomes' measure.

NCT ID: NCT04821804 Completed - Clinical trials for Gingival Recession, Plastic Surgery

Local Application of Hyaluronic Acid (HYADENT BG) With Free Soft Tissue Grafing Improves Treatment Outcomes.

Start date: January 2, 2020
Phase: Phase 2/Phase 3
Study type: Interventional

A total of 24 healthy non-smoker patients requiring FGG recruited for the study. Subjects were equally and randomly assigned into two groups. Test group, local application of HYADENT BG on both donor and recipient sites. Control group, application of normal saline on both sites as placebo. The FGG dimensions were evaluated at 1, 3- and 6-month recall using digital photographs. Post-operative pain was evaluated for 14 days. Color matching and patient satisfaction were evaluated at 6 months.