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NCT ID: NCT04467892 Completed - Clinical trials for Ventilator Associated Pneumonia

Low Versus High Corticosteroid Use in Ventilator Associated Pneumonia

Start date: January 2, 2018
Phase: Phase 2
Study type: Interventional

patients who had >3 on Murray score and >6 on CPIS allocated randomly in two groups 120 patients in each. Group A received 30 mg/kg methyl-prednisolone slowly intravenous in 250 mL normal saline every 8 hours for only 48 hours while group B received 1 mg/kg/day methyl-prednisolone divided to three doses given every 8 hours for two weeks. Duration of the study last 16 days, Morbidity considered if no improvement in any or all clinical parameters of both Murray and CPIS scores and failure of weaning of patients from the ventilator at the studied period.

NCT ID: NCT04464408 Completed - COVID-19 Clinical Trials

Favipiravir Therapy in Adults With Mild COVID-19

Avi-Mild
Start date: July 23, 2020
Phase: Phase 2/Phase 3
Study type: Interventional

Favipiravir is a selective and potent inhibitor of influenza viral RNA polymerase. It acts as a purine analogue, which selectively inhibits viral RNA-dependent RNA polymerase (RdRps). It has the characteristic of acting on RNA viruses including Ebola and Coronaviruses especially novel coronavirus (2019-nCoV). The purpose of this study is to evaluate the clinical efficacy and safety of Favipiravir in comparison to placebo in the treatment of mild COVID-19 cases. It is a Multicenter, randomized double-blinded, parallel-group trial.

NCT ID: NCT04463199 Completed - Neck Pain Clinical Trials

Effects of Deep Cervical Flexors Training On Forward Head Posture, Neck Pain and Functional Status

Start date: February 20, 2019
Phase: N/A
Study type: Interventional

Using computer for long hours is related to higher risk of computer related muscular disorders like forward head posture and neck pain. Deep cervical flexor muscles are important head-on-neck posture stabilizers thus their training may lead to improvement in forward head posture (FHP) and neck pain (NP).

NCT ID: NCT04463186 Completed - Muscle Strength Clinical Trials

Time Based Effects of Different Duration Stretching on Calf Muscle Strength

Start date: January 30, 2019
Phase: N/A
Study type: Interventional

Stretching is reported to decrease muscle strength and thus suggested to be avoided prior to athletic events but with conflicting reports. This time course study aimed to assess acute effects of static stretching of different durations on isometric maximum voluntary contraction force of calf muscle.

NCT ID: NCT04453644 Completed - STRETCHING Clinical Trials

Effects of Stretching on Strength of Proximal and Distal Group of Muscles - A Comparative Study

Start date: January 23, 2019
Phase: N/A
Study type: Interventional

Muscular flexibility is believed to prevent injuries and improve movement therefore most coaches include stretching exercises in their pre-competition and pre-exercise warm-up routines. One question arises here, should sports persons avoid stretching exercises prior to sporting events thereby exposing themselves to musculoskeletal injuries, or should they continue stretching exercises prior to sporting events and risk losing the maximal performance? The aim of this study is to compare the effects of 2, 4, and 8 min of static stretching (SS) on isometric maximum voluntary contraction (MVCF) force between proximal (Hamstrings) and distal group (Calf) of muscles.

NCT ID: NCT04448288 Completed - Stretch Clinical Trials

Time-based Effects of Stretching on Hamstrings Muscle Strength

Start date: January 30, 2019
Phase: N/A
Study type: Interventional

Stretching is reported to have detrimental effects on strength and thus avoided prior to strength training session. Do stretching indeed decreases muscle strength? To examine the time course (immediate, 10- and 20-min post stretching) for the effects of 2, 4, and 8 min long duration of static-stretching (SS) on isometric maximum voluntary contraction (MVC) force of hamstring muscles.

NCT ID: NCT04427046 Completed - Clinical trials for Acute Myocardial Infarction

Acute Myocardial Infarction in Native Versus Non-native Young Population in Saudi Arabia

YAMI
Start date: June 9, 2020
Phase:
Study type: Observational

A retrospective study collecting the data of young patients admitted with diagnosis of Acute Myocardial Infarction.

NCT ID: NCT04424563 Completed - Traumatic Bleeding Clinical Trials

Activated Factor Seven in Traumatic Retro Peritoneal Hematoma

Start date: May 5, 2017
Phase:
Study type: Observational [Patient Registry]

80 patients with traumatic retro-peritoneal hematoma allocated into two groups 40 patients each. Patients of Group A received aminocaproic acid while patients of group B received aFVII. Number of packed RBCs given to get target Hb level and time to get this target Hb level (>10 gm%) recorded as indicators for control bleeding. Blood pressure, pulse, Arterial blood gasses and urine output recorded as indicator for treatment of hypovolemic shock. hypoxic index, chest X ray and coagulation profile used as indicator for complication.

NCT ID: NCT04411160 Completed - ARDS Clinical Trials

Vitamin C Versus Nitric Oxide in Prolonged Ventilation

Start date: January 15, 2019
Phase:
Study type: Observational

This a prospective double-blind study done in King Abdul-Aziz specialist hospital between January 2019 and April 2020 in the intensive care unit on 60 patients with difficult weaning and ventilated for 10 days. Allocated randomly in two groups 30 patients in each. All patients in both groups continued on the same conventional ventilation but Group A received nitric oxide (NO) while group B received vitamin C intravenous. The duration of the study last 16 days. during this period, APCHII score, Hemodynamics, Chest Xray, hypoxic index, lung compliance, Recruitment maneuver, arterial blood saturation, LDH, C-reactive protein used as indicator for improvement. Number of patients weaned from the ventilator and patients died also recorded.

NCT ID: NCT04406506 Completed - Clinical trials for Postoperative Nausea

Entral Feeding in Acute Severe Pancreatitis

Start date: June 10, 2018
Phase:
Study type: Observational [Patient Registry]

• A total of 60 patients admitted to King Abdulaziz Specialists Hospital between June 2018 and April 2020 with both a clinical and biochemical presentation of acute pancreatitis with the following inclusion criteria: Abdominal pain > 6 on the visual analogue scale without given analgesia , abdominal distension and tenderness with serum amylase and serum lipase at least 3 times the upper limit of the reference range (considering normal lipase level from 0-160 U/L, and normal amylase level from 0-100 U/L) with confirmed abdominal computerized axial tomography of grade D and E on Ranson and colleagues criteria(28) of inflamed pancreatic picture.