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NCT ID: NCT04270747 Completed - Clinical trials for Neovascular (Wet) Age-related Macular Degeneration (AMD)

A Study to Understand Effectiveness and Safety of ABP 938 Compared to Aflibercept (Eylea®) in Patients Suffering With Neovascular Age-related Macular Degeneration [Neovascular (Wet) AMD]

Start date: June 22, 2020
Phase: Phase 3
Study type: Interventional

The purpose of this study is to compare the efficacy and safety of ABP 938 versus Aflibercept (Eylea®) in the treatment of neovascular age-related macular degeneration. Subjects will be randomized in a masked 1:1 ratio to receive 2 mg (0.05 mL) of either ABP 938 (Treatment Group A) or aflibercept (Treatment Group B) administered by intravitreal (IVT) injection.

NCT ID: NCT04270669 Completed - Clinical trials for Wet Age-Related Macular Degeneration

Evaluation of RC28-E Injection in Wet Age-related Macular Degeneration

Start date: April 15, 2020
Phase: Phase 1/Phase 2
Study type: Interventional

This is a non-randomized, open-label, multicenter, 48-week study to investigate the efficacy, safety and pharmacokinetics of RC28-E injection in the treatment of patients with wet age-related macular degeneration by multiple administration.

NCT ID: NCT04270331 Completed - Pain Clinical Trials

Assessment and Management of Pain, Agitation, Delirium and Sleep Deprivation (PADS) in ICU by PADS Protocol, Thailand

Start date: April 1, 2020
Phase: N/A
Study type: Interventional

The investigators proposed that pain, agitation, delirium and sleep deprivation protocol (PADS) will help improve the patients' outcomes (shortening ICU length of stay, improving ventilator free days, increasing delirium free days) in critically ill patients, a university hospital, Thailand.

NCT ID: NCT04269837 Completed - Clinical trials for Malignant Female Reproductive System Neoplasm

Sexual Health Counseling Intervention During Radiation Therapy in Improving Quality of Life for Women With Gynecologic Cancer

Start date: May 20, 2021
Phase: N/A
Study type: Interventional

This phase I trial studies a sexual health counseling intervention during radiation therapy in improving quality of life for women with gynecologic cancer. Women with gynecologic cancer often suffer long-term complications from treatment that can affect their physical and psychological well-being. An early sexual health counseling intervention prior to and after radiation may improve symptoms management and reduce the physical and psychological effects of treatment.

NCT ID: NCT04269564 Completed - Clinical trials for Atelectasis, Postoperative Pulmonary

Optimizing PEEP in Laparoscopic Bariatric Surgery Using Bedside Lung Ultrasound

Start date: February 20, 2020
Phase: N/A
Study type: Interventional

Lung ultrasound imaging is a promising non-invasive, non-radiant, portable and easy to use tool that as yet to be studied in the intraoperative setting. in our current study, we are trying to reach the optimum PEEP in laparoscopic bariatric patients to prevent postoperative collapse and atlectasis with simple non-invasive procedure.

NCT ID: NCT04269408 Completed - Clinical trials for Aneurysmal Subarachnoid Hemorrhage

A Safety and Efficacy Study of NicaPlant® in Aneurysmal Subarachnoid Haemorrhage Patients Undergoing Aneurysm Clipping

Start date: April 5, 2020
Phase: Phase 2
Study type: Interventional

This study of NicaPlant® is conducted in patients who have a subarachnoid haemorrhage. Patients will be randomized in two treatment groups. Both groups will receive the standard of care and the investigational group will receive in addition NicaPlant®. NicaPlant® is tested to reduce the long-term complications of aneurysmal subarachnoid haemorrhage (aSAH).

NCT ID: NCT04269122 Completed - Clinical trials for Ornithine Transcarbamylase Deficiency

A Study to Assess Plasma Ammonia Time-Normalized Area Under the Curve and Rate of Ureagenesis in Healthy Adult Subjects

Start date: August 2, 2019
Phase:
Study type: Observational

The objective of the study is to characterize 24-hour plasma ammonia levels, characterize urea production rates in healthy normal subjects.

NCT ID: NCT04268641 Completed - Clinical trials for Hemiplegia and/or Hemiparesis Following Stroke

Evaluation of Positioning Protocols on a Wheelchair in Hemiplegic Patients

POSIT-HEMI
Start date: August 28, 2020
Phase: N/A
Study type: Interventional

The main purpose of this study is to assess the interest of using wheelchair positioning equipment on the decrease of postural disorders, compared to the standard use of a wheelchair

NCT ID: NCT04268628 Completed - Clinical trials for Metastatic Castration-resistant Prostate Cancer

A Study of Pharmacodynamic and Genetic Parameters of Abira-DES Study Participants (NCT02217566) - Participants With Metastatic Castration-Resistant Prostate Cancer Treated With Abiraterone Acetate Following Unresponsive Treatment With Diethylstilbestrol

EXPLORE
Start date: March 19, 2020
Phase:
Study type: Observational

The primary purpose of this study is to evaluate the influence of HSD3B1 (1245C) germline variant and potential pharmacodynamic markers on abiraterone activity in participants with metastatic castration-resistant prostate cancer after unresponsive use of diethylstilbestrol.

NCT ID: NCT04268251 Completed - Clinical trials for Cavernous Sinus Invasion by Pituitary Adenoma

Evaluation of Cavernous Sinus Invasion by Pituitary Adenoma Using Deep Learning Based Denoising MR

Start date: January 12, 2020
Phase: N/A
Study type: Interventional

Preoperative evaluation of cavernous sinus invasion by pituitary adenoma is critical for performing safe operation and deciding on surgical extent as well as for treatment success. Because of the small size of the pituitary gland and sellar fossa, determining the exact relationship between the pituitary adenoma and cavernous sinus can be challenging. Performing thin slice thickness MRI may be beneficial but is inevitably associated with increased noise level. By applying deep learning based denoising algorithm, diagnosis of cavernous sinus invasion by pituitary adenoma may be improved.