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NCT ID: NCT03161184 Completed - Clinical trials for Obstetric Complication

Impact of a Smartphone Intervention on Tanzanian Women's Childbirth Location

SUSTAIN1
Start date: July 23, 2013
Phase: N/A
Study type: Interventional

This study investigates whether training Community Health Workers (CHW) to use a smartphone-based prenatal counseling application as a "job aid" instead of the existing paper based standard is associated with increased women's use of maternal health services in Singida region, Tanzania.

NCT ID: NCT03160911 Completed - Ulcer Bleeding Clinical Trials

The Use of Over-the-scope-clip for Prevention of Rebleeding in High Risk Peptic Ulcers

Start date: March 16, 2018
Phase: N/A
Study type: Interventional

Non-variceal acute gastrointestinal bleeding is a common and potentially life-threatening problem. The conventional treatment of this condition is for esophagogastroduodenoscopy (OGD) for haemostasis. Treatment methods include heater probe, clipping and injection of adrenaline. Recently, a new device called the Over-the-scope clip (OTSC) has been device to treat perforations and bleeding in the gastrointestinal tract. Therefore, the aim of the study is to compare between the treatment outcomes between OTSC and conventional endoscopic haemostatic methods in ulcers that are of high risk for rebleeding.

NCT ID: NCT03160820 Completed - Measles Clinical Trials

Study on Immunization Schedule of Beijing Tiantan Biological's Measles-mumps-rubella(MMR) Vaccine

Start date: March 2016
Phase: Phase 4
Study type: Interventional

This study will evaluate the immunogenicity and safety of Beijing Tiantan's MMR vaccine in subjects 18 months of age and older. The MMR vaccine may be administered as a second dose to 4-6 year-old persons with one dose immunization with MMR vaccine or as a first dose to 18 month-old subjects with one dose immunization with measles-rubella(MR).

NCT ID: NCT03160495 Completed - Clinical trials for Squamous Cell Carcinoma of the Head and Neck

Functional ImaGing of Heterogeneity in Head and Neck Tumors - Validation From Surgical Specimens

FIGHHT
Start date: March 29, 2017
Phase:
Study type: Observational [Patient Registry]

The purpose of this study is to investigate if heterogeneity in head and neck squamous cell carcinoma as seen in functional imaging with PET/MR can be correlated to biologic heterogeneity in surgical specimens.

NCT ID: NCT03160209 Completed - Clinical trials for Esophageal Squamous Cell Carcinoma

HIV and Other Risk Factors for Esophageal Squamous Cell Carcinoma in Malawi

Start date: July 26, 2017
Phase:
Study type: Observational

The primary purpose of this single-center, case-control, non-interventional study is to determine risk factors which contribute to the development of esophageal squamous cell carcinoma (ESCC) at Kamuzu Central Hospital (KCH) and St. Gabriel Hospital (SGH) in Malawi.

NCT ID: NCT03160144 Completed - Clinical trials for Respiratory Insufficiency

The PROtective Ventilation Using Open Lung Approach Or Not Trial

PROVOLON
Start date: January 12, 2017
Phase: N/A
Study type: Interventional

Postoperative Pulmonary Complications (PPC) are very common. It severely affects postoperative recovery, particularly in the abdominal surgery. Patients with laparoscopic resection of colorectal cancer generally have a higher age and decreased lung function reserve. At the same time, they prone to developing atelectasis due to the effects of pneumoperitoneum pressure. Therefore, they are a high-risk group of respiratory insufficiency and PPC. Mechanical ventilation with a low tidal volume is a routine in clinic nowadays. However, this conventional strategy will also result in atelectasis formation. Therefore, it may deteriorate the vulnerable lung function of patients undergoing laparoscopic resection of colorectal cancer. Patients with Acute Lung Injury or Acute Respiratory Distress Syndrome (ALI/ARDS) could benefit from the "open lung approach", including the use of positive end-expiratory pressure (PEEP) and recruitment maneuvers (RMs). Whether a lung protective mechanical ventilation strategy with medium levels of PEEP and repeated RMs, the "open lung approach", protects against respiratory insufficiency and PPC during laparoscopic resection of colorectal cancer is uncertain. The present study aims at comparing the effects of "open lung approach" mechanical ventilation strategy and conventional mechanical ventilation strategy in PPC, extra-pulmonary complications, length of hospital stay, biomarkers of lung injury and changes of respiratory function in patients undergoing general anesthesia for laparoscopic resection of colorectal cancer.

NCT ID: NCT03160040 Completed - Clinical trials for Gram-Negative Bacterial Infections

A Retrospective Observational Study to Evaluate the Utilization, Outcomes, and Adverse Events in Participants Treated With Minocin® (Minocycline) for Infections Caused by Gram-negative Bacteria in a Real World Setting

Start date: October 11, 2017
Phase:
Study type: Observational

This study is a retrospective, observational study to evaluate minocycline use in participants under real world conditions.

NCT ID: NCT03159845 Completed - Clinical trials for Stem Cell Transplant Complications

Zinc as Enhancer in Immune Recovery After Stem Cell Transplantation for Hematological Malignancies

ZENITH
Start date: January 1, 2014
Phase: Phase 2
Study type: Interventional

Patients affected by multiple myeloma undergone autologous stem cell transplantation (SCT) are enrolled at the moment of stem cell collection. They are randomized 1:1 in two groups at the moment of the graft. Patients of the Control group take only standard antimicrobial prophylaxis after SCT; the Sample group takes in addition a daily oral supplementation of Zinc Sulfate (600 mg/die) from day +5 until day +100 after SCT. Laboratory tests are performed on peripheral blood samples.

NCT ID: NCT03159611 Completed - Clinical trials for Sequelae of Perinatal Brain Injury

Efficacy and Safety Clinical Trial of Tenoten for Children Liquid Dosage Form Therapy in Infants With Sequelae of Perinatal Brain Injury

Start date: February 19, 2016
Phase: Phase 3
Study type: Interventional

Purpose of the study: - To assess the clinical efficacy of Tenoten for children liquid dosage form therapy (10 oral drops per day for 12 weeks) in Infants with Sequelae of Perinatal Brain Injury (mild-to-moderate cerebral hypoxia-ischaemia and/or mild-to-moderate intracranial haemorrhage). - To assess the safety of Tenoten for children liquid dosage form therapy (10 oral drops per day for 12 weeks) in Infants with Sequelae of Perinatal Brain Injury (mild-to-moderate cerebral hypoxia-ischaemia and/or mild-to-moderate intracranial haemorrhage).

NCT ID: NCT03159520 Completed - Clinical trials for Orthodontic Appliance Complication

Control of Pain From Braces With Patient Advice Sheets

COPPAS
Start date: June 27, 2017
Phase: N/A
Study type: Interventional

To compare the analgesic property of acupressure with NSAIDs (Ibuprofen) in controlling pain following orthodontic treatment. This will be achieved by assessing the effectiveness of acupressure in controlling pain and discomfort by measuring the degree of pain relief after bonding of brackets to teeth and placement of initial archwire.