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NCT ID: NCT04721002 Completed - Clinical trials for Multiple Myeloma (MM)

Study to Evaluate t(11;14) Status and BCL2 Expression in Adult Participants With Multiple Myeloma (MM)

MEDICI
Start date: July 7, 2021
Phase:
Study type: Observational

Multiple myeloma (MM) is a rare cancer caused by abnormal survival of plasma cells (blood cells). Most trial participants with MM relapse (cancer has come back) or become non- responsive to treatment and remission gets shorter after each line of treatment. This is a study to assess t(11;14) and BCL2 expression in adult participants with newly diagnosed and relapsed/refractory (R/R) MM. Approximately 500 adult participants with newly confirmed or relapsed/refractory (R/R) multiple myeloma (MM) will be enrolled in around 15-20 countries. Participants will receive standard of care while participating in this study. No drug will be administered as a part of this study. Participants will attend regular visits during the course of the study at a hospital or clinic and will be asked to provide bone marrow and blood samples.

NCT ID: NCT04718259 Completed - Analgesia Clinical Trials

The Use of Midazolam as Adjuvant to Bupivacaine Intrathecal Anesthesia for Children Undergoing Lower Abdominal Surgeries.

Start date: January 18, 2020
Phase: Early Phase 1
Study type: Interventional

The study will be carried on children undergoing lower abdominal surgeries. Patients will be randomly categorized into two study groups. Group A will include patients who will receive bupivacaine intrathecal injection without adjuvant. Group B will include patients who will receive bupivacaine and preservative-free midazolam.

NCT ID: NCT04713423 Completed - Clinical trials for Herpes Simplex Virus Infection

Oral and Perioral Herpes Simplex Virus Infection Type I in a Five-month-old Infant: A Case Report

Start date: October 19, 2017
Phase:
Study type: Observational

A five-month-old healthy girl who presented with painful herpetic gingivostomatitis and perioral vesicles.

NCT ID: NCT04692142 Completed - Clinical trials for Educational Problems

A Cross-over Randomised Trial Comparing Two Teaching Methods

Start date: August 30, 2020
Phase: N/A
Study type: Interventional

The aim of the study aim to test the null hypothesis which states that there are no significant differences in knowledge retention and exam performance of dental undergraduate students in a Saudi Dental School using two different asynchronous teaching methods . The secondary aim is to analyse students' perceptions to the two teaching methods.

NCT ID: NCT04686123 Completed - Postural; Defect Clinical Trials

Efficacy of a Supervised Intervention Protocol on Rounded Shoulder Posture and Shoulder ROM Among Saudi Young Females

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

Shortening of pectoralis minor (PMi) muscle affects the scapular excursion that results in limited shoulder flexion range of motion (SFROM). The purpose is to evaluate the effect of Stretching of PM muscle along with the strengthening of lower trapezius (LTR) muscle to increase the length of PM muscle (PML) and limited SFROM in young adult females with rounded shoulder posture.

NCT ID: NCT04680923 Completed - Pain, Postoperative Clinical Trials

Efficacy of CPPLAI in Laparoscopic Sleeve Gastrectomy Patients

CPPLAI
Start date: December 8, 2020
Phase: N/A
Study type: Interventional

The high demand for bariatric surgery due to the increasing prevalence of obesity worldwide necessitate evidence-based clinical pathway such as Enhanced Recovery After Bariatric Surgery (ERABS). The paradigm of surgery has been shifted from open to laparoscopic in morbidly obese patients. Laparoscopic Sleeve Gastrectomy (LSG) is the most common procedure performed in our institute for sustained weight loss and amelioration of obesity-related comorbidities. Pain control in ERABS is one of the key factors for improved outcomes. Surgery induced acute postoperative pain, stress response and fatigue lead to prolonged convalescence and hospital stay. Optimal titrated safe postoperative pain management in LSG patients still remains a challenge.

NCT ID: NCT04673500 Completed - Clinical trials for Injection Site Irritation

Assessment of Pain on Propofol Injection.

Start date: May 2013
Phase: N/A
Study type: Interventional

Title: Assessment of pain on lidocaine-Propofol admixture injection: Comparing large antecubital vein and small vein dorsum of hand. - Objective: To evaluate the pain on Propofol - lidocaine admixture injection using different sizes of veins on upper limb. - Design: Prospective randomized clinical trial Place and duration of study: Department of Anesthesia, King Saud University Riyadh May 1, 2013 - May 31, 2014). - Patient and methods: Total 160 adult patients were divided in two groups. Age 20-50 years of either gender, American Society of Anesthesiologist (ASA) class 1 and 2, scheduled for elective surgery under general anesthesia were included in the study. Patients with known history of allergy to lidocaine or Propofol, obese patients, anticipated difficult intubation, already on any analgesics and pregnant patients were excluded from the study. Both groups received an admixture of Propofol (1%) - lidocaine (2%) on induction of anesthesia through antecubital vein (Group- 1) or through a vein on dorsum of hand (Group- 2). Pain was assessed as none, mild, moderate or severe. Results: Moderate to severe pain on intravenous injection of Propofol-lidocaine admixture through antecubital vein and small vein on dorsum of hand was 20% vs 71%. Conclusion: There is marked reduction of pain when Propofol - lidocaine admixture was injected through antecubital vein as compared to small vein on dorsum of hand. - Key words: Propofol, injection, pain

NCT ID: NCT04671927 Completed - Pathway Lesions Clinical Trials

Assessment of Anterior Visual Pathway Lesions: Prospective Descriptive Study

MRCT
Start date: February 1, 2019
Phase:
Study type: Observational

This study describe and compare the role of computed tomography (CT) and magnetic resonance imaging (MRI) in the evaluation of anterior visual pathway lesions. A prospective descriptive study conducted on 30 patients with symptoms related to visual pathway (13 females and 17 males; mean age 30.7 ± 8.2 years; range 4-70 years). Considering anatomical site of lesions, our patients were subdivided into three main groups: optic nerve lesions (n= 9), optic chiasm lesions (n= 17), and lesions involving optic tract and lateral geniculate body (n= 4). The imaging findings of CT and MRI were described and compared.

NCT ID: NCT04669327 Completed - Clinical trials for Scoliosis Idiopathic

Hip and Knee Moments Normal and With Scoliosis

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

Kinetic analysis appears to be useful in providing objective information regarding the gait abilities of scoliotic patients which is difficult to be observed in a clinical setting. Objective: the aim of the study was to analyze the hip and knee peak abductor moments during gait in subjects with idiopathic scoliosis.

NCT ID: NCT04663516 Completed - Fatigue Clinical Trials

Effectiveness of Exercise Through Video Games in Reducing Fatigue Among Children With Leukemia

Start date: September 1, 2019
Phase: N/A
Study type: Interventional

40 children with cancer who fulfills the inclusion criteria will be included. Participants will be recruited from King Fahad Children's Cancer Center, King Fahad Medical City and King Khaled University Hospital. After obtaining written formal consent, children will be randomly assigned to two groups, control and experimental. Experimental group will play 60 minutes of Wii physical activity games for three weeks, twice each week. while control group will receive conventional therapy. Fatigue will be assessed using pediatric multidimensional fatigue scale- child proxy before, weekly during the study and after. Functional capacity will be measured by six minute walk test before and after study duration, and physical activity will be repeatedly measured by godin-shephard leisure time physical activity questionnaire. All data will be analyzed using appropriate statistical analysis.